Canonical Allele Identifier: PA2827923085
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1735851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Met1295Thr
CA062435
NM_001354701.2:c.3884T>C