Canonical Allele Identifier: PA2825941894
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ala1329Pro
CA017704
NM_001160160.2:c.3985G>C