ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA1139765582
Gene: FTCD
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_996848.1:p.Ala159Val
CA10073855
NM_206965.2:c.476C>T