Canonical Allele Identifier: PA2573205658
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1506327
ClinVar RCV Id: RCV002006647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Tyr165Ser
CA2573136124
NM_001354723.2:c.494A>C