Allele Registry

Canonical Allele Identifier: PA645453674

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000484396

RCV001061560

ClinVar Variation:

421864

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Met1476Thr	CA16620554 NM_000334.4:c.4427T>C