Canonical Allele Identifier: PA2830300891
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2136916
ClinVar RCV Id: RCV003037351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Asp239Gly
CA377509791
NM_152871.4:c.716A>G