Canonical Allele Identifier: PA2826085271
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Gly255Asp
CA136932
NM_001173425.1:c.764G>A