Allele Registry

Canonical Allele Identifier: PA916005145

Gene: FGF12 HGNC NCBI

ClinVar RCV:

RCV000258032

RCV000522341

RCV001249217

RCV002294210

ClinVar Variation:

266034

HGVS (amino-acid)	Matching Registered Transcripts
NP_004104.3:p.Arg52His	CA10588956 NM_004113.6:c.155G>A