Canonical Allele Identifier: PA2573311521
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1471706
ClinVar RCV Id: RCV001975708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Asp92Asn
CA351750750
NM_198156.3:c.274G>A