Canonical Allele Identifier: PA2580120047
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2127762
ClinVar RCV Id: RCV003055654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Met213Val
CA1247597
NM_000639.3:c.637A>G