Allele Registry

Canonical Allele Identifier: PA2825190701

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV002006886

ClinVar Variation:

1506651

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Ser43Cys	CA351748024 NM_000551.4:c.128C>G