Allele Registry

Canonical Allele Identifier: PA645484055

Gene: FGF12 HGNC NCBI

ClinVar RCV:

RCV000258032

RCV000522341

RCV001249217

RCV002294210

ClinVar Variation:

266034

HGVS (amino-acid)	Matching Registered Transcripts
NP_066360.1:p.Arg114His	CA10588956 NM_021032.5:c.341G>A