Canonical Allele Identifier: PA2573311302
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1371900
ClinVar RCV Id: RCV001864672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Leu48Gln
CA351748198
NM_198156.3:c.143T>A