Canonical Allele Identifier: PA2573063609
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1327546
ClinVar RCV Id: RCV001789808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Cys202Ser
CA343806213
NM_000639.3:c.604T>A
CA343806217
NM_000639.3:c.605G>C