Allele Registry

Canonical Allele Identifier: PA2830430638

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001526916

ClinVar Variation:

1172856

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Gln123Lys	CA351756143 NM_198156.3:c.367C>A