Canonical Allele Identifier: PA1139676954
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 958243
ClinVar RCV Id: RCV001231369 RCV002484264
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu160Gln
CA351756093
NM_000551.4:c.478G>C