Allele Registry

Canonical Allele Identifier: PA1139765018

Gene: FAS HGNC NCBI

ClinVar RCV:

RCV001047921

ClinVar Variation:

844948

HGVS (amino-acid)	Matching Registered Transcripts
NP_690611.1:p.Thr214Ile	CA5593175 NM_152872.4:c.641C>T CA916080419 NM_152872.4:c.641_642delinsTC