Canonical Allele Identifier: PA2825190502
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1017783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gly14Ser
CA351747168
NM_000551.4:c.40G>A