Canonical Allele Identifier: PA2826914822
Gene: CCT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2398858
ClinVar RCV Id: RCV004233607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293085.1:p.Pro126Ser
CA359181523
NM_001306156.2:c.376C>T