Canonical Allele Identifier: PA2830430907
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2937784
ClinVar RCV Id: RCV003794414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.His150Tyr
CA351756416
NM_198156.3:c.448C>T