Canonical Allele Identifier: PA916025161
Gene: FGF14 HGNC NCBI

Linked Data

ClinVar Variation Id: 8115
ClinVar RCV Id: RCV002472354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308876.1:p.Phe98Ser
CA254318
NM_001321947.2:c.293T>C