Allele Registry

Canonical Allele Identifier: PA2825214520

Gene: FASLG HGNC NCBI

ClinVar Allele:

1153360

ClinVar RCV:

RCV001522939

RCV002283549

RCV003326584

ClinVar Variation:

1170509

HGVS (amino-acid)	Matching Registered Transcripts
NP_000630.1:p.Phe87Leu	CA1247490 NM_000639.3:c.259T>C CA343805419 NM_000639.3:c.261T>A CA343805420 NM_000639.3:c.261T>G