Allele Registry

Canonical Allele Identifier: PA2826471033

Gene: CLPB HGNC NCBI

ClinVar Allele:

185680

ClinVar RCV:

RCV000167539

ClinVar Variation:

187782

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245321.1:p.Ala561Val	CA198522 NM_001258392.1:c.1682C>T