Allele Registry

Canonical Allele Identifier: PA2830430941

Gene: VHL HGNC NCBI

ClinVar Allele:

393232

ClinVar RCV:

RCV000476155

RCV002356706

RCV004001993

ClinVar Variation:

411991

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Lys155Glu	CA16611099 NM_198156.3:c.463A>G