Canonical Allele Identifier: PA2825944772
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Asp1221Asn
CA017530
NM_001160161.2:c.3661G>A