Canonical Allele Identifier: PA2825190647
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1303980
ClinVar RCV Id: RCV001758273 RCV001861065
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu37Asp
CA351747799
NM_000551.4:c.111G>C
CA351747806
NM_000551.4:c.111G>T