Canonical Allele Identifier: PA2825944729
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Asp1189Asn
CA017472
NM_001160161.2:c.3565G>A