Canonical Allele Identifier: PA658799991
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 526669
ClinVar Variation Id: 1392637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Lys171Asn
CA351756203
NM_000551.4:c.513G>C
CA351756204
NM_000551.4:c.513G>T