Allele Registry

Canonical Allele Identifier: PA2573311270

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV002006886

ClinVar Variation:

1506651

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Ser43Cys	CA351748024 NM_198156.3:c.128C>G