Allele Registry

Canonical Allele Identifier: PA2741815301

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV003787095

ClinVar Variation:

2928273

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Thr133Ser	CA351753978 NM_000551.4:c.397A>T CA351753986 NM_000551.4:c.398C>G