Canonical Allele Identifier: PA2499303368
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1006593
ClinVar RCV Id: RCV001303659 RCV002341603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro40Ala
CA351747889
NM_198156.3:c.118C>G