Canonical Allele Identifier: PA915962854
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 650472
ClinVar RCV Id: RCV000805632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Ile168Asn
CA343805998
NM_000639.3:c.503T>A