Canonical Allele Identifier: PA2573205654
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1414331
ClinVar RCV Id: RCV001928631
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Thr164Ala
CA2573136123
NM_001354723.2:c.490A>G