Canonical Allele Identifier: PA2825191259
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 857493
ClinVar RCV Id: RCV001063174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro102Ser
CA040238
NM_000551.4:c.304C>T