Canonical Allele Identifier: PA2826471631
Gene: CLPB HGNC NCBI

Linked Data

ClinVar Variation Id: 235218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245323.1:p.Ser178Asn
CA6171478
NM_001258394.1:c.533G>A