Canonical Allele Identifier: PA1139725113
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 937160
ClinVar RCV Id: RCV001206119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Asn557Ser
CA374621160
NM_015404.4:c.1670A>G