Canonical Allele Identifier: PA2826085441
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 914596
ClinVar RCV Id: RCV001168834 RCV001168835 RCV001236567
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Gly389Glu
CA5206064
NM_001173425.1:c.1166G>A