Canonical Allele Identifier: PA916056860
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411986
ClinVar RCV Id: RCV000459599 RCV002411515
ClinVar Variation Id: 2954421
ClinVar RCV Id: RCV003813644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Glu6Asp
CA16611153
NM_198156.3:c.18G>T
CA351747037
NM_198156.3:c.18G>C