Allele Registry

Canonical Allele Identifier: PA254661

Gene: FGF8 HGNC NCBI

ClinVar RCV:

RCV000009695

ClinVar Variation:

9125

HGVS (amino-acid)	Matching Registered Transcripts
NP_149353.1:p.Arg127Gly	CA254660 NM_033163.4:c.379C>G