Allele Registry

Canonical Allele Identifier: PA341674

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000020273

RCV000992897

ClinVar Variation:

21157

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Met1370Val	CA341673 NM_000334.4:c.4108A>G