Canonical Allele Identifier: PA645462577
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 238113
ClinVar RCV Id: RCV000231328 RCV000412262 RCV001026150 RCV003463663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gly24Asp
CA10582111
NM_000551.4:c.71G>A