Canonical Allele Identifier: PA2827044720
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1627789
ClinVar RCV Id: RCV002133000
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307341.1:p.Gly336Val
CA10073624
NM_001320412.2:c.1007G>T