Canonical Allele Identifier: PA2825943135
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Arg104Gly
CA016820
NM_001160161.2:c.310C>G