Allele Registry

Canonical Allele Identifier: PA211322

Gene: FTL HGNC NCBI

ClinVar RCV:

RCV000144502

RCV000311515

RCV000395171

RCV000861621

RCV003103735

RCV003323416

ClinVar Variation:

156439

HGVS (amino-acid)	Matching Registered Transcripts
NP_000137.2:p.Glu57Lys	CA211321 NM_000146.4:c.169G>A