Canonical Allele Identifier: PA658669291
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 480772
ClinVar RCV Id: RCV000561095 RCV001553667 RCV001224534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu163Phe
CA351756135
NM_000551.4:c.487C>T