Canonical Allele Identifier: PA2580120175
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1996327
ClinVar RCV Id: RCV002823705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Tyr218Cys
CA343806327
NM_000639.3:c.653A>G