Allele Registry

Canonical Allele Identifier: PA113665

Gene: FGF14 HGNC NCBI

ClinVar RCV:

RCV002472354

ClinVar Variation:

8115

HGVS (amino-acid)	Matching Registered Transcripts
NP_004106.1:p.Phe145Ser	CA254318 NM_004115.4:c.434T>C