Canonical Allele Identifier: PA2825515272
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2092717
ClinVar RCV Id: RCV003018339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077354.2:p.Asn176His
CA5205857
NM_001083885.3:c.526A>C