Canonical Allele Identifier: PA2825190697
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1043302
ClinVar RCV Id: RCV001347390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu42Gly
CA351747982
NM_000551.4:c.125A>G