Canonical Allele Identifier: PA2825494445
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Thr843Ala
CA016243
NM_001099405.2:c.2527A>G