Allele Registry

Canonical Allele Identifier: PA2580476087

Gene: CAB39L HGNC NCBI

ClinVar RCV:

RCV004162937

ClinVar Variation:

2314258

HGVS (amino-acid)	Matching Registered Transcripts
NP_112187.2:p.Met258Leu	CA249322295 NM_030925.4:c.772A>C CA388175168 NM_030925.4:c.772A>T