Canonical Allele Identifier: PA162663
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 135405
ClinVar RCV Id: RCV000122259 RCV000199012 RCV000565432 RCV000662921 RCV001588971 RCV003153403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro40Leu
CA020046
NM_000551.4:c.119C>T