Canonical Allele Identifier: PA2742030743
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2934338
ClinVar RCV Id: RCV003796088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro103Ser
CA351751072
NM_198156.3:c.307C>T