Canonical Allele Identifier: PA2827924059
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 179372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg1910His
CA019464
NM_001354701.2:c.5729G>A