Canonical Allele Identifier: PA2580556370
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2167790
ClinVar RCV Id: RCV003092741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro59Leu
CA351748662
NM_198156.3:c.176C>T