Canonical Allele Identifier: PA916029078
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45648
ClinVar RCV Id: RCV000038866 RCV001168064 RCV001168063 RCV001206517
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333819.1:p.Arg99His
CA136870
NM_001346890.1:c.296G>A