Canonical Allele Identifier: PA2580120025
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2092369
ClinVar RCV Id: RCV003016067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Arg198Trp
CA343806189
NM_000639.3:c.592C>T