Allele Registry

Canonical Allele Identifier: PA2580249431

Gene: FAM153A HGNC NCBI

ClinVar RCV:

RCV004132513

ClinVar Variation:

2283646

HGVS (amino-acid)	Matching Registered Transcripts
NP_001381268.1:p.Glu242Asp	CA3587026 NM_001394339.1:c.726G>C CA362618430 NM_001394339.1:c.726G>T