Canonical Allele Identifier: PA2825939998
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg53Gln
CA015041
NM_001160160.2:c.158G>A