Canonical Allele Identifier: PA916056913
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 420914
ClinVar RCV Id: RCV000485486 RCV001020464 RCV000808373 RCV003464013 RCV004003340
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Glu12Gln
CA16617779
NM_198156.3:c.34G>C