Allele Registry

Canonical Allele Identifier: PA645453461

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000414860

RCV001070785

RCV001566689

ClinVar Variation:

374058

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Ala699Thr	CA16043536 NM_000334.4:c.2095G>A