Canonical Allele Identifier: PA2825132649
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 406444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1896Gln
CA064637
NM_000335.5:c.5687G>A