Canonical Allele Identifier: PA2741815443
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2937784
ClinVar RCV Id: RCV003794414
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.His191Tyr
CA351756416
NM_000551.4:c.571C>T