Canonical Allele Identifier: PA1139668139
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 939692
ClinVar RCV Id: RCV001209128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu199Val
CA351756563
NM_000551.4:c.596A>T