Canonical Allele Identifier: PA2827921200
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg27His
CA019812
NM_001354701.2:c.80G>A