Allele Registry

Canonical Allele Identifier: PA112200

Gene: FTL HGNC NCBI

ClinVar Allele:

31525

ClinVar RCV:

RCV000017950

ClinVar Variation:

16486

HGVS (amino-acid)	Matching Registered Transcripts
NP_000137.2:p.Ala96Thr	CA281022 NM_000146.4:c.286G>A