Allele Registry

Canonical Allele Identifier: PA2573062277

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV001787411

ClinVar Variation:

1327128

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Ser682Trp	CA8709667 NM_000334.4:c.2045C>G