Canonical Allele Identifier: PA2825943708
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Gly514Cys
CA014960
NM_001160161.2:c.1540G>T