Canonical Allele Identifier: PA2827386756
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 199137
ClinVar RCV Id: RCV000218629 RCV000724324 RCV003947539
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333819.1:p.Val384Ile
CA248169
NM_001346890.1:c.1150G>A