Canonical Allele Identifier: PA2826471560
Gene: CLPB HGNC NCBI

Linked Data

ClinVar Variation Id: 384218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245322.1:p.Thr647Ala
CA6170972
NM_001258393.1:c.1939A>G