Canonical Allele Identifier: PA2827091636
Gene: FGF14 HGNC NCBI

Linked Data

ClinVar Variation Id: 807035
ClinVar RCV Id: RCV000995076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308860.1:p.Gly90Arg
CA388711172
NM_001321931.1:c.268G>A
CA388711173
NM_001321931.1:c.268G>C