Allele Registry

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Canonical Allele Identifier: PA2825190684

Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1757751

ClinVar RCV Id: RCV002370945

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Glu41Asp	CA351747945 NM_000551.4:c.123A>T CA351747951 NM_000551.4:c.123A>C