Canonical Allele Identifier: PA916056031
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 646267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Val1287Ala
CA352148254
NM_198056.3:c.3860T>C