Allele Registry

Canonical Allele Identifier: PA2828710113

Gene: FGF12 HGNC NCBI

ClinVar RCV:

RCV000258032

RCV000522341

RCV001249217

RCV002294210

ClinVar Variation:

266034

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364223.1:p.Arg28His	CA10588956 NM_001377294.1:c.83G>A