Allele Registry

Canonical Allele Identifier: PA149682

Gene: FTL HGNC NCBI

ClinVar Allele:

102582

ClinVar RCV:

RCV000082857

RCV001857397

RCV003884347

ClinVar Variation:

96689

HGVS (amino-acid)	Matching Registered Transcripts
NP_000137.2:p.Met1Val