Canonical Allele Identifier: PA357014
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223166
ClinVar RCV Id: RCV000208790 RCV000469401 RCV000679023 RCV002444839 RCV003389711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Phe76del
CA357012
NM_000551.4:c.227_229del
CA2573320343
NM_000551.4:c.227_228delinsAA