Canonical Allele Identifier: PA2825943137
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 850004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ser106Gly
CA352157035
NM_001160161.2:c.316A>G