Canonical Allele Identifier: PA2742029665
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2584499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Lys1477Thr
CA352145222
NM_198056.3:c.4430A>C