Canonical Allele Identifier: PA136871
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_056219.3:p.Arg450His
CA136870
NM_015404.4:c.1349G>A