Allele Registry

Canonical Allele Identifier: PA2830431066

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000767299

ClinVar Variation:

625270

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Asp172_Ter173insCysArgPheLeuLeuLysLeuThrLeuPheHisLeuSerPhe	CA351756722 NM_198156.3:c.519A>C CA351756724 NM_198156.3:c.519A>T