Canonical Allele Identifier: PA2830300886
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 860668
ClinVar RCV Id: RCV001067019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Ile238Thr
CA377509786
NM_152871.4:c.713T>C