Canonical Allele Identifier: PA204247
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val1667Ile
CA018825
NM_001099404.2:c.4999G>A