Allele Registry

Canonical Allele Identifier: PA2828131054

Gene: CLTB HGNC NCBI

ClinVar RCV:

RCV004138154

ClinVar Variation:

2283049

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351056.1:p.Pro16Leu	CA3568910 NM_001364127.2:c.47C>T