Allele Registry

Canonical Allele Identifier: PA2573063610

Gene: FASLG HGNC NCBI

ClinVar RCV:

RCV001789805

ClinVar Variation:

1327543

HGVS (amino-acid)	Matching Registered Transcripts
NP_000630.1:p.Ala247Glu	CA1247609 NM_000639.3:c.740C>A