Canonical Allele Identifier: PA645458050
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 293734
ClinVar RCV Id: RCV000356098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Ala93Val
CA1247494
NM_000639.3:c.278C>T