Allele Registry

Canonical Allele Identifier: PA2830300779

Gene: FAS HGNC NCBI

ClinVar RCV:

RCV001047921

ClinVar Variation:

844948

HGVS (amino-acid)	Matching Registered Transcripts
NP_690610.1:p.Thr193Ile	CA5593175 NM_152871.4:c.578C>T CA916080419 NM_152871.4:c.578_579delinsTC