Allele Registry

Canonical Allele Identifier: PA2827926843

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000034799

RCV000693265

RCV002426542

RCV003996180

ClinVar Variation:

41865

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Asn90Ser	CA020212 NM_001354723.2:c.269A>G