Canonical Allele Identifier: PA2825489524
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1735851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Met1296Thr
CA062435
NM_001099404.2:c.3887T>C