Canonical Allele Identifier: PA335678
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 216476
ClinVar RCV Id: RCV000195431 RCV000409910 RCV000492641 RCV001582695 RCV003462330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ala5Val
CA039495
NM_000551.4:c.14C>T