Canonical Allele Identifier: PA2825538339
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 451632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val836Met
CA060533
NM_001099404.2:c.2506G>A