Canonical Allele Identifier: PA916056849
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 574321
ClinVar RCV Id: RCV000696229 RCV002334321 RCV000997984 RCV003999652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro2Ser
CA70042126
NM_198156.3:c.4C>T