Canonical Allele Identifier: PA2825190474
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1005487
ClinVar RCV Id: RCV001302369
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu10Gly
CA351747095
NM_000551.4:c.29A>G