Allele Registry

Canonical Allele Identifier: PA2829344075

Gene: CLTB HGNC NCBI

ClinVar RCV:

RCV004138154

ClinVar Variation:

2283049

HGVS (amino-acid)	Matching Registered Transcripts
NP_001825.1:p.Pro16Leu	CA3568910 NM_001834.3:c.47C>T