Allele Registry

Canonical Allele Identifier: PA1139676849

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001221169

ClinVar Variation:

949664

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Asp121Val	CA351753756 NM_000551.4:c.362A>T