Canonical Allele Identifier: PA2826471915
Gene: CLPB HGNC NCBI

Linked Data

ClinVar Variation Id: 187781
ClinVar RCV Id: RCV000167538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245323.1:p.Gly601Val
CA198520
NM_001258394.1:c.1802G>T