Canonical Allele Identifier: PA2825190680
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1373310
ClinVar RCV Id: RCV001880717 RCV004009241 RCV004040589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro40Ser
CA351747893
NM_000551.4:c.118C>T