Canonical Allele Identifier: PA2825190790
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2949244
ClinVar RCV Id: RCV003801970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Met54Ile
CA351748478
NM_000551.4:c.162G>A
CA351748485
NM_000551.4:c.162G>C
CA351748488
NM_000551.4:c.162G>T