Canonical Allele Identifier: PA1139676836
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 862346
ClinVar RCV Id: RCV001069048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Trp117Gly
CA351753662
NM_000551.4:c.349T>G