Canonical Allele Identifier: PA2827044756
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1376953
ClinVar RCV Id: RCV001888248
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307341.1:p.Ala439del
CA2580615224
NM_001320412.2:c.1314_1316del