Canonical Allele Identifier: PA2827092019
Gene: FGF14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2849354
ClinVar RCV Id: RCV003695683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308865.1:p.Leu98Trp
CA388711263
NM_001321936.1:c.293T>G