Canonical Allele Identifier: PA112210
Gene: FTL HGNC NCBI

Linked Data

ClinVar Variation Id: 39583
ClinVar RCV Id: RCV000032783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000137.2:p.Thr30Ile
CA130378
NM_000146.4:c.89C>T