Canonical Allele Identifier: PA645462568
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 420914
ClinVar RCV Id: RCV000485486 RCV001020464 RCV000808373 RCV003464013 RCV004003340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu12Gln
CA16617779
NM_000551.4:c.34G>C