Canonical Allele Identifier: PA2580120042
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1715711
ClinVar RCV Id: RCV002301448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Lys210Glu
CA343806270
NM_000639.3:c.628A>G