Canonical Allele Identifier: PA184294
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 179372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg1929His
CA019464
NM_001099404.2:c.5786G>A