Canonical Allele Identifier: PA2825945590
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Asp1736Gly
CA019174
NM_001160161.2:c.5207A>G