Canonical Allele Identifier: PA308016
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asp651His
CA015631
NM_001099404.2:c.1951G>C