Canonical Allele Identifier: PA2580138253
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2011881
ClinVar RCV Id: RCV002838743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077354.2:p.Ala5Thr
CA374609736
NM_001083885.3:c.13G>A