Allele Registry

Canonical Allele Identifier: PA645458052

Gene: FASLG HGNC NCBI

ClinVar RCV:

RCV000329844

RCV004021376

ClinVar Variation:

293736

HGVS (amino-acid)	Matching Registered Transcripts
NP_000630.1:p.His122Asn	CA1247528 NM_000639.3:c.364C>A