Canonical Allele Identifier: PA265752
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ala1698Thr
CA018875
NM_001099404.2:c.5092G>A