Canonical Allele Identifier: PA916057049
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 421185
ClinVar RCV Id: RCV000481405 RCV001071961 RCV002395163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Ala50Val
CA039477
NM_198156.3:c.149C>T