Canonical Allele Identifier: PA2825190674
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1006593

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro40Ala
CA351747889
NM_000551.4:c.118C>G