Canonical Allele Identifier: PA2829647088
Gene: FTCD HGNC NCBI
ClinVar RCV:
RCV003058988
ClinVar Variation:
2142288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006648.1:p.Ala360Thr
CA410513261
NM_006657.3:c.1078G>A