Canonical Allele Identifier: PA2825942779
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg1886His
CA064762
NM_001160160.2:c.5657G>A