Canonical Allele Identifier: PA2825492277
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1941987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Thr163Ile
CA352154025
NM_001099405.2:c.488C>T