Canonical Allele Identifier: PA2830300946
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2001711
ClinVar RCV Id: RCV002815652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Gln255His
CA377509904
NM_152871.4:c.765A>C
CA377509905
NM_152871.4:c.765A>T