Canonical Allele Identifier: PA2826471072
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_001245321.1:p.Gly616Val
CA198520
NM_001258392.1:c.1847G>T