Canonical Allele Identifier: PA2827091875
Gene: FGF14 HGNC NCBI

Linked Data

ClinVar Variation Id: 8115
ClinVar RCV Id: RCV002472354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308863.1:p.Phe61Ser
CA254318
NM_001321934.1:c.182T>C