Canonical Allele Identifier: PA2825942797
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 179372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg1896His
CA019464
NM_001160160.2:c.5687G>A