Canonical Allele Identifier: PA2825130573
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1213747
ClinVar RCV Id: RCV001591696
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Thr1056Ala
CA352139207
NM_000335.5:c.3166A>G