Allele Registry

Canonical Allele Identifier: PA2826742334

Gene: CAB39L HGNC NCBI

ClinVar RCV:

RCV004162937

ClinVar Variation:

2314258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274267.1:p.Met258Leu	CA249322295 NM_001287338.1:c.772A>C CA388175168 NM_001287338.1:c.772A>T