Allele Registry

Canonical Allele Identifier: PA645453389

Gene: SCN4A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

361025

442007

ClinVar RCV:

RCV000414792

RCV000415234

RCV000516348

RCV000559054

RCV000626662

RCV001197414

RCV004527624

ClinVar Variation:

373945

448262

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000325.4:p.Val445Leu	CA16043537 NM_000334.4:c.1333G>T CA400635022 NM_000334.4:c.1333G>C