Canonical Allele Identifier: PA2830430697
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2218
ClinVar RCV Id: RCV000002302 RCV000002303 RCV000132159 RCV000213079 RCV000435817 RCV000627746 RCV000763092 RCV003992144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Arg126Trp
CA020450
NM_198156.3:c.376C>T