Canonical Allele Identifier: PA2573101001
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1311412
ClinVar RCV Id: RCV001752395
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro71Leu
CA351749021
NM_198156.3:c.212C>T