Allele Registry

Canonical Allele Identifier: PA2827926457

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000459599

RCV002411515

RCV003813644

ClinVar Variation:

411986

2954421

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Glu6Asp	CA16611153 NM_001354723.2:c.18G>T CA351747037 NM_001354723.2:c.18G>C