Canonical Allele Identifier: PA658799999
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 526677
ClinVar RCV Id: RCV000631274 RCV000679044 RCV000767296 RCV002343200
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro192Leu
CA351756444
NM_000551.4:c.575C>T