Canonical Allele Identifier: PA2825945646
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ala1774Thr
CA019290
NM_001160161.2:c.5320G>A