Allele Registry

Canonical Allele Identifier: PA645453560

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000418825

RCV000528478

ClinVar Variation:

384521

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Val1230Met	CA8709207 NM_000334.4:c.3688G>A