Allele Registry

Canonical Allele Identifier: PA2825191914

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000767299

ClinVar Variation:

625270

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Asp213_Ter214insCysArgPheLeuLeuLysLeuThrLeuPheHisLeuSerPhe	CA351756722 NM_000551.4:c.642A>C CA351756724 NM_000551.4:c.642A>T