Allele Registry

Canonical Allele Identifier: PA341740

Gene: FASLG HGNC NCBI

ClinVar RCV:

RCV000020369

RCV002476995

ClinVar Variation:

21212

HGVS (amino-acid)	Matching Registered Transcripts
NP_000630.1:p.Arg156Gly	CA341738 NM_000639.3:c.466A>G