Allele Registry

Canonical Allele Identifier: PA916012598

Gene: FGF8 HGNC NCBI

ClinVar RCV:

RCV000009695

ClinVar Variation:

9125

HGVS (amino-acid)	Matching Registered Transcripts
NP_006110.1:p.Arg98Gly	CA254660 NM_006119.6:c.292C>G