Allele Registry

Canonical Allele Identifier: PA350904

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000206912

ClinVar Variation:

221262

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Arg1448Ser	CA350903 NM_000334.4:c.4342C>A