Allele Registry

Canonical Allele Identifier: PA2499233383

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001526916

ClinVar Variation:

1172856

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Gln164Lys	CA351756143 NM_000551.4:c.490C>A