Canonical Allele Identifier: PA2825190995
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 648755
ClinVar RCV Id: RCV000803557 RCV002442677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ile75Met
CA351749213
NM_000551.4:c.225C>G