Canonical Allele Identifier: PA2825495794
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 265302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg1309Cys
CA10588360
NM_001099405.2:c.3925C>T