Canonical Allele Identifier: PA1139676855
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 861319
ClinVar RCV Id: RCV001067824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ala122Gly
CA351753773
NM_000551.4:c.365C>G