Canonical Allele Identifier: PA264866
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67630
ClinVar RCV Id: RCV000058386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly351Val
CA014246
NM_000335.5:c.1052G>T