Canonical Allele Identifier: PA2825495845
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ala1330Pro
CA017704
NM_001099405.2:c.3988G>C