Allele Registry

Canonical Allele Identifier: PA645462980

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000492347

ClinVar Variation:

428808

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Thr133Pro	CA351753973 NM_000551.4:c.397A>C