Canonical Allele Identifier: PA2825191174
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1504644
ClinVar RCV Id: RCV002028959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asp92Ala
CA351750762
NM_000551.4:c.275A>C