Canonical Allele Identifier: PA330020
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Leu1283Met
CA017562
NM_001099404.2:c.3847C>A