Canonical Allele Identifier: PA2829647077
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1627789
ClinVar RCV Id: RCV002133000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006648.1:p.Gly336Val
CA10073624
NM_006657.3:c.1007G>T