Canonical Allele Identifier: PA2573171686
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1468713
ClinVar RCV Id: RCV001969130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Gln200Lys
CA343806199
NM_000639.3:c.598C>A