Canonical Allele Identifier: PA108969
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2233
ClinVar RCV Id: RCV000002321 RCV000115744 RCV000213077 RCV000418681 RCV000656990 RCV001080004 RCV002467489 RCV001843451 RCV003225718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro81Ser
CA020148
NM_000551.4:c.241C>T