Allele Registry

Canonical Allele Identifier: PA645462538

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000462197

RCV000574549

RCV001053669

RCV001356021

ClinVar Variation:

411973

849658

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Asn7Lys	CA16611156 NM_000551.4:c.21C>A CA351747053 NM_000551.4:c.21C>G