Canonical Allele Identifier: PA307091
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg27His
CA019812
NM_001099404.2:c.80G>A