Canonical Allele Identifier: PA265483
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val1405Met
CA017946
NM_001099404.2:c.4213G>A