Canonical Allele Identifier: PA2580120046
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1985077
ClinVar RCV Id: RCV002800440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Val211Ile
CA1247595
NM_000639.3:c.631G>A