Allele Registry

Canonical Allele Identifier: PA645458050

Gene: FASLG HGNC NCBI

ClinVar RCV:

RCV000356098

ClinVar Variation:

293734

HGVS (amino-acid)	Matching Registered Transcripts
NP_000630.1:p.Ala93Val	CA1247494 NM_000639.3:c.278C>T