Allele Registry

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Canonical Allele Identifier: PA2825190518

Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1052300

ClinVar RCV Id: RCV001360453 RCV001773713 RCV002341754

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Glu17Asp	CA351747259 NM_000551.4:c.51G>C CA351747262 NM_000551.4:c.51G>T