Allele Registry

Canonical Allele Identifier: PA645453656

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000313533

RCV000344057

RCV000368322

RCV000392378

RCV000405474

RCV002502255

RCV003137925

ClinVar Variation:

324517

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Val1442Met	CA8708993 NM_000334.4:c.4324G>A