NM_206933.4(USH2A):c.3811+19_3811+20del AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 2, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003810657.2
Allele description [Variation Report for NM_206933.4(USH2A):c.3811+19_3811+20del]
NM_206933.4(USH2A):c.3811+19_3811+20del
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
CNAG_07527 [Cryptococcus neoformans var. grubii H99]
CNAG_07527 [Cryptococcus neoformans var. grubii H99]Gene ID:23890365Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024