Allele Registry

Canonical Allele Identifier: PA3057575817

Gene: FASLG HGNC NCBI

ClinVar RCV:

RCV000017959

RCV001789750

ClinVar Variation:

16495

HGVS (amino-acid)	Matching Registered Transcripts
NP_000630.1:p.Met158_Glu185del	CA126563 NM_000639.3:c.473_556del