Canonical Allele Identifier: PA2742030567
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2949244
ClinVar RCV Id: RCV003801970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Met54Ile
CA351748478
NM_198156.3:c.162G>A
CA351748485
NM_198156.3:c.162G>C
CA351748488
NM_198156.3:c.162G>T