Canonical Allele Identifier: PA2825945747
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 180517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Pro1837Ala
CA019410
NM_001160161.2:c.5509C>G