Canonical Allele Identifier: PA916057161
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 419821
ClinVar RCV Id: RCV000485402 RCV001851172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Asn67His
CA16617785
NM_198156.3:c.199A>C