Canonical Allele Identifier: PA2829647098
Gene: FTCD HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006648.1:p.Gly380Arg
CA410512877
NM_006657.3:c.1138G>C
CA410512878
NM_006657.3:c.1138G>A