Allele Registry

Canonical Allele Identifier: PA645453586

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000725970

RCV001362169

ClinVar Variation:

287216

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Phe1298Cys	CA10605700 NM_000334.4:c.3893T>G