Canonical Allele Identifier: PA2826471116
Gene: CLPB HGNC NCBI

Linked Data

ClinVar Variation Id: 384218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245321.1:p.Thr676Ala
CA6170972
NM_001258392.1:c.2026A>G