Canonical Allele Identifier: PA174777
Gene: FAXC HGNC NCBI

Linked Data

ClinVar Variation Id: 161783
ClinVar RCV Id: RCV000149319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115900.1:p.Gln298Glu
CA174776
NM_032511.2:c.892C>G