Canonical Allele Identifier: PA2825496977
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Val1745Met
CA019062
NM_001099405.2:c.5233G>A