Allele Registry

Canonical Allele Identifier: PA2830366866

Gene: FAM153A HGNC NCBI

ClinVar RCV:

RCV004132513

ClinVar Variation:

2283646

HGVS (amino-acid)	Matching Registered Transcripts
NP_775934.3:p.Glu165Asp	CA3587026 NM_173663.5:c.495G>C CA362618430 NM_173663.5:c.495G>T