NM_015937.6(PIGT):c.167C>T (p.Ser56Leu) AND Multiple congenital anomalies-hypotonia-seizures syndrome 3
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001908757.4
-
septin-2 isoform a [Homo sapiens]
septin-2 isoform a [Homo sapiens]gi|56549636|ref|NP_001008491.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023