Canonical Allele Identifier: PA2825190439
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 655972
ClinVar RCV Id: RCV000812261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asn7Thr
CA351747046
NM_000551.4:c.20A>C