Canonical Allele Identifier: PA1139758693
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 923735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.His558Cys
CA1139655765
NM_198056.3:c.1672_1673delinsTG