Canonical Allele Identifier: PA916073841
Gene: FTCD HGNC NCBI
ClinVar RCV:
RCV000350124
ClinVar Variation:
340419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996848.1:p.Arg446Gln
CA10073478
NM_206965.2:c.1337G>A