Allele Registry

Canonical Allele Identifier: PA2826771986

Gene: NFIL3 HGNC NCBI

ClinVar RCV:

RCV004207485

ClinVar Variation:

2369783

HGVS (amino-acid)	Matching Registered Transcripts
NP_001276929.1:p.Ala146Ser	CA5120121 NM_001290000.2:c.436G>T