Canonical Allele Identifier: PA2580569207
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2142288
ClinVar RCV Id: RCV003058988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996848.1:p.Ala360Thr
CA410513261
NM_206965.2:c.1078G>A