Canonical Allele Identifier: PA2830430822
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1014559
ClinVar RCV Id: RCV001313310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Arg135Ser
CA041381
NM_198156.3:c.405G>T
CA351756237
NM_198156.3:c.405G>C