Canonical Allele Identifier: PA2829647160
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1402273
ClinVar RCV Id: RCV001906356
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006648.1:p.Ser460Leu
CA410558949
NM_006657.3:c.1379C>T