Canonical Allele Identifier: PA2825515188
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_001077354.2:p.Arg67His
CA136870
NM_001083885.3:c.200G>A