Canonical Allele Identifier: PA916057252
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro81Ser
CA020148
NM_198156.3:c.241C>T