Allele Registry

Canonical Allele Identifier: PA645453677

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000427535

ClinVar Variation:

380391

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Leu1488Pro	CA16607427 NM_000334.4:c.4463T>C