Canonical Allele Identifier: PA2825945828
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 978333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Glu1884Asp
CA352139848
NM_001160161.2:c.5652A>T
CA352139850
NM_001160161.2:c.5652A>C