Canonical Allele Identifier: PA916057249
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 36899
ClinVar RCV Id: RCV000030582 RCV000129974 RCV001034657 RCV001547784 RCV003460493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro81Leu
CA020154
NM_198156.3:c.242C>T