Canonical Allele Identifier: PA2829823430
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2011881
ClinVar RCV Id: RCV002838743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Ala388Thr
CA374609736
NM_015404.4:c.1162G>A