Canonical Allele Identifier: PA916057160
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 625221
ClinVar RCV Id: RCV000767233
ClinVar Variation Id: 1784514
ClinVar RCV Id: RCV002417451 RCV003101012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Asn67Lys
CA039757
NM_198156.3:c.201C>G
CA351748855
NM_198156.3:c.201C>A