Canonical Allele Identifier: PA164309
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 141044
ClinVar RCV Id: RCV000129380 RCV000663314 RCV000631273 RCV000679037 RCV001007623 RCV003155081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asp126Asn
CA020313
NM_000551.4:c.376G>A