Canonical Allele Identifier: PA350901
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 221263
ClinVar RCV Id: RCV000518944 RCV000206910
JSON-LD

Amino-acid Alleles

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