Canonical Allele Identifier: PA916073794
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 4017
ClinVar RCV Id: RCV000004232
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996848.1:p.Arg135Cys
CA116584
NM_206965.2:c.403C>T