Canonical Allele Identifier: PA2826471096
Gene: CLPB HGNC NCBI

Linked Data

ClinVar Variation Id: 279613
ClinVar RCV Id: RCV000258936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245321.1:p.Ile652Asn
CA10602723
NM_001258392.1:c.1955T>A