Canonical Allele Identifier: PA2573171684
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1479824
ClinVar RCV Id: RCV001991044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Trp162Arg
CA343805952
NM_000639.3:c.484T>A
CA343805953
NM_000639.3:c.484T>C