Canonical Allele Identifier: PA1139674305
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 837364
ClinVar RCV Id: RCV001038680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Gln220Arg
CA343806340
NM_000639.3:c.659A>G