Canonical Allele Identifier: PA2827044762
Gene: FTCD HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307341.1:p.Arg446Gln
CA10073478
NM_001320412.2:c.1337G>A