Canonical Allele Identifier: PA2499305782
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1005867
ClinVar RCV Id: RCV001302815 RCV003166707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996848.1:p.Arg477Trp
CA10073442
NM_206965.2:c.1429C>T