Allele Registry

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Canonical Allele Identifier: PA2573311327

Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1377127

ClinVar RCV Id: RCV001889835

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Glu53Asp	CA351748440 NM_198156.3:c.159G>T CA351748444 NM_198156.3:c.159G>C