Canonical Allele Identifier: PA2573317061
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1355344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996848.1:p.Ala455Thr
CA10073469
NM_206965.2:c.1363G>A