Canonical Allele Identifier: PA2825943995
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ala691Thr
CA015822
NM_001160161.2:c.2071G>A