Canonical Allele Identifier: PA916020353
Gene: CCT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1327
ClinVar RCV Id: RCV000001390 RCV000434241 RCV003952334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293083.1:p.His92Arg
CA114935
NM_001306154.2:c.275A>G