Allele Registry

Canonical Allele Identifier: PA658668855

Gene: SCN4A HGNC NCBI

ClinVar RCV:

RCV000539082

RCV001548373

RCV002526745

ClinVar Variation:

477405

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Ala734Ser	CA8709637 NM_000334.4:c.2200G>T