Canonical Allele Identifier: PA2573286479
Gene: CLPB HGNC NCBI

Linked Data

ClinVar Variation Id: 1676588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110440.1:p.Gly560Arg
CA381726572
NM_030813.6:c.1678G>C
CA381726574
NM_030813.6:c.1678G>A