Allele Registry

Canonical Allele Identifier: PA915960392

Gene: VHL HGNC NCBI

ClinVar Allele:

807496

ClinVar RCV:

RCV001023797

RCV001359453

RCV001536627

ClinVar Variation:

825586

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Tyr175Phe	CA351756230 NM_000551.4:c.524A>T