Canonical Allele Identifier: PA658799969
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 526681
ClinVar RCV Id: RCV000631278 RCV001766342
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asp126His
CA351753833
NM_000551.4:c.376G>C