Canonical Allele Identifier: PA136929
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45681
ClinVar RCV Id: RCV000038899 RCV000279685 RCV000316099 RCV000839182
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Arg223His
CA136928
NM_015404.4:c.668G>A