Canonical Allele Identifier: PA2826086222
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_001166896.1:p.Arg877Gln
CA5205565
NM_001173425.1:c.2630G>A