Canonical Allele Identifier: PA2825515164
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 937102
ClinVar RCV Id: RCV001206050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077354.2:p.Gly27Ser
CA5206007
NM_001083885.3:c.79G>A