Allele Registry

Canonical Allele Identifier: PA2830430664

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000767279

ClinVar Variation:

625253

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Gln123Glu	CA351756145 NM_198156.3:c.367C>G