Allele Registry

Canonical Allele Identifier: PA2825191039

Gene: VHL HGNC NCBI

ClinVar Allele:

1304491

ClinVar RCV:

RCV001771461

RCV001868619

RCV004040282

ClinVar Variation:

1314230

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Pro81Gln	CA351750529 NM_000551.4:c.242C>A