Canonical Allele Identifier: PA2827091632
Gene: FGF14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2849354
ClinVar RCV Id: RCV003695683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308860.1:p.Leu77Trp
CA388711263
NM_001321931.1:c.230T>G