Canonical Allele Identifier: PA2830301051
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2004873
ClinVar RCV Id: RCV002820611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Val314_Ter315insTyrSerGluLysGlnGlnIleGlnPhe
CA377510312
NM_152871.4:c.945G>C
CA377510313
NM_152871.4:c.945G>T