Allele Registry

Canonical Allele Identifier: PA2825191042

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001379600

ClinVar Variation:

1068142

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Pro81Ala	CA351750524 NM_000551.4:c.241C>G