Canonical Allele Identifier: PA2829647143
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 645399
ClinVar RCV Id: RCV000799465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006648.1:p.Ala438Thr
CA410559496
NM_006657.3:c.1312G>A