Canonical Allele Identifier: PA184293
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 179372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1928His
CA019464
NM_000335.5:c.5783G>A