Canonical Allele Identifier: PA658669118
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 486722
ClinVar RCV Id: RCV000563088
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ala18Ser
CA351747273
NM_000551.4:c.52G>T