Allele Registry

Canonical Allele Identifier: PA645453507

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000438769

RCV001058903

ClinVar Variation:

281372

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Asp1069Asn	CA8709348 NM_000334.4:c.3205G>A