Canonical Allele Identifier: PA2825191913
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223236
ClinVar RCV Id: RCV000208844 RCV003765350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asp213_Ter214insLeuArgPheLeuLeuLysLeuThrLeuPheHisLeuSerPhe
CA357103
NM_000551.4:c.641G>T