Canonical Allele Identifier: PA1139752422
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 920699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ala60Pro
CA352158329
NM_198056.3:c.178G>C