Canonical Allele Identifier: PA2825495676
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Asp1275Asn
CA017530
NM_001099405.2:c.3823G>A