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Canonical Allele Identifier: Get Identifier
Gene: FTCD HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996848.1:p.Ser261Arg
CA10073706
NM_206965.2:c.781A>C
CA410516489
NM_206965.2:c.783C>G
CA410516490
NM_206965.2:c.783C>A