Canonical Allele Identifier: PA2829647193
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2954983
ClinVar RCV Id: RCV003816182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006648.1:p.Ala525Val
CA410555622
NM_006657.3:c.1574C>T