Canonical Allele Identifier: PA2573170901
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1472969
ClinVar RCV Id: RCV001977317 RCV003320863 RCV003170281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gln203Lys
CA351756610
NM_000551.4:c.607C>A