Allele Registry

Canonical Allele Identifier: PA916056901

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000554589

RCV000764457

RCV001019152

ClinVar Variation:

456583

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Ala11Pro	CA351747101 NM_198156.3:c.31G>C