Canonical Allele Identifier: PA2826471959
Gene: CLPB HGNC NCBI

Linked Data

ClinVar Variation Id: 384218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245323.1:p.Thr661Ala
CA6170972
NM_001258394.1:c.1981A>G