Canonical Allele Identifier: PA113665
Gene: FGF14 HGNC NCBI

Linked Data

ClinVar Variation Id: 8115
ClinVar RCV Id: RCV002472354

Amino-acid Alleles

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