Canonical Allele Identifier: PA916057471
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223193
ClinVar RCV Id: RCV000208843 RCV003765349
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Val114Leu
CA357101
NM_198156.3:c.340G>C
CA351751376
NM_198156.3:c.340G>T