Canonical Allele Identifier: PA2827091877
Gene: FGF14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2461207
ClinVar RCV Id: RCV003179739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308863.1:p.Ile72Val
CA388711302
NM_001321934.1:c.214A>G