Canonical Allele Identifier: PA2742037592
Gene: FTCD HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996848.1:p.Gly380Arg
CA410512877
NM_206965.2:c.1138G>C
CA410512878
NM_206965.2:c.1138G>A