Canonical Allele Identifier: PA2830358474
Gene: FGF14 HGNC NCBI

Linked Data

ClinVar Variation Id: 807035
ClinVar RCV Id: RCV000995076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_787125.1:p.Gly179Arg
CA388711172
NM_175929.3:c.535G>A
CA388711173
NM_175929.3:c.535G>C