Canonical Allele Identifier: PA2825945806
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Ala1870Thr
CA019460
NM_001160161.2:c.5608G>A