Canonical Allele Identifier: PA2827091933
Gene: FGF14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2461207
ClinVar RCV Id: RCV003179739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308864.1:p.Ile72Val
CA388711302
NM_001321935.1:c.214A>G