Canonical Allele Identifier: PA645462696
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 231233
ClinVar RCV Id: RCV000213269 RCV000631267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro59Ser
CA10578179
NM_000551.4:c.175C>T