Canonical Allele Identifier: PA2827386870
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 912452
ClinVar RCV Id: RCV001165661 RCV001165662 RCV001324966
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333819.1:p.Arg527Gln
CA5205565
NM_001346890.1:c.1580G>A