Canonical Allele Identifier: PA211805
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1957Gln
CA019519
NM_000335.5:c.5870G>A