Canonical Allele Identifier: PA2825190534
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1442279
ClinVar RCV Id: RCV001969825 RCV003892994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gly19Val
CA351747296
NM_000551.4:c.56G>T