Canonical Allele Identifier: PA2825940335
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asp297Asn
CA019914
NM_001160160.2:c.889G>A