Allele Registry

Canonical Allele Identifier: PA2826471874

Gene: CLPB HGNC NCBI

ClinVar Allele:

185680

ClinVar RCV:

RCV000167539

ClinVar Variation:

187782

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245323.1:p.Ala546Val	CA198522 NM_001258394.1:c.1637C>T