ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2580569213
Gene: FTCD
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_996848.1:p.Ala418Thr
CA10073582
NM_206965.2:c.1252G>A