Canonical Allele Identifier: PA645458049
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 293732
ClinVar RCV Id: RCV000260218 RCV004021375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Pro59Leu
CA1247469
NM_000639.3:c.176C>T