Allele Registry

Canonical Allele Identifier: PA110784

Gene: FTCD HGNC NCBI

ClinVar RCV:

RCV000004233

ClinVar Variation:

4018

HGVS (amino-acid)	Matching Registered Transcripts
NP_006648.1:p.Arg299Pro	CA116585 NM_006657.3:c.896G>C