Canonical Allele Identifier: PA2825191207
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1426321
ClinVar RCV Id: RCV001931250
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gln96Thr
CA2573136088
NM_000551.4:c.286_288delinsACC