Canonical Allele Identifier: PA2825190678
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2934082
ClinVar RCV Id: RCV003795832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro40Gln
CA351747894
NM_000551.4:c.119C>A