Canonical Allele Identifier: PA2825943333
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 569420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Val258Ala
CA352150816
NM_001160161.2:c.773T>C