Allele Registry

Canonical Allele Identifier: PA350901

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000206910

RCV000518944

ClinVar Variation:

221263

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Arg1448Pro	CA350900 NM_000334.4:c.4343G>C