Allele Registry

Canonical Allele Identifier: PA2827092817

Gene: FGF14 HGNC NCBI

ClinVar RCV:

RCV002472354

ClinVar Variation:

8115

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308874.1:p.Phe111Ser	CA254318 NM_001321945.2:c.332T>C