Canonical Allele Identifier: PA2830430863
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1368873
ClinVar RCV Id: RCV001894758 RCV004009230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Arg141Met
CA351756317
NM_198156.3:c.422G>T