Allele Registry

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Canonical Allele Identifier: PA2829647165

Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1443575

ClinVar RCV Id: RCV001955675 RCV002562866

ClinVar Variation Id: 2360577

ClinVar RCV Id: RCV002989566

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_006648.1:p.Ala464Val	CA10073454 NM_006657.3:c.1391C>T CA2573157738 NM_006657.3:c.1391_1392delinsTG