Canonical Allele Identifier: PA108950
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2234
ClinVar RCV Id: RCV000002322 RCV000236065 RCV000704063 RCV001024480 RCV002490296 RCV003996075
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro192Ser
CA020501
NM_000551.4:c.574C>T