Canonical Allele Identifier: PA2742037582
Gene: FTCD HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996848.1:p.Thr47Ser
CA10074052
NM_206965.2:c.140C>G
CA410522532
NM_206965.2:c.139A>T