Canonical Allele Identifier: PA2830430914
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2234
ClinVar RCV Id: RCV000002322 RCV000236065 RCV000704063 RCV001024480 RCV002490296 RCV003996075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro151Ser
CA020501
NM_198156.3:c.451C>T