Canonical Allele Identifier: PA110774
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 4017
ClinVar RCV Id: RCV000004232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006648.1:p.Arg135Cys
CA116584
NM_006657.3:c.403C>T