Allele Registry

Canonical Allele Identifier: PA280294

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000030585

RCV000679036

ClinVar Variation:

36902

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Thr124Ile	CA020308 NM_000551.4:c.371C>T