ClinGen Allele Registry
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Canonical Allele Identifier:
PA645458052
Gene: FASLG
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
277642
ClinVar RCV:
RCV000329844
RCV004021376
ClinVar Variation:
293736
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000630.1:p.His122Asn
CA1247528
NM_000639.3:c.364C>A