Canonical Allele Identifier: PA2825190921
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2931182
ClinVar RCV Id: RCV003782444
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asn67Thr
CA351748831
NM_000551.4:c.200A>C