Allele Registry

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Canonical Allele Identifier: PA2827926735

Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 625221

ClinVar RCV Id: RCV000767233

ClinVar Variation Id: 1784514

ClinVar RCV Id: RCV002417451 RCV003101012

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Asn67Lys	CA039757 NM_001354723.2:c.201C>G CA351748855 NM_001354723.2:c.201C>A