Canonical Allele Identifier: PA2827377539
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_001333459.1:p.Gln177Glu
CA174776
NM_001346530.2:c.529C>G