Canonical Allele Identifier: PA645453661
Gene: CLPB HGNC NCBI

Linked Data

ClinVar Variation Id: 279613
ClinVar RCV Id: RCV000258936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110440.1:p.Ile682Asn
CA10602723
NM_030813.6:c.2045T>A