Canonical Allele Identifier: PA2827926784
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1011133
ClinVar RCV Id: RCV001308893
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Cys77Ser
CA351749264
NM_001354723.2:c.229T>A
CA351749273
NM_001354723.2:c.230G>C