Allele Registry

Canonical Allele Identifier: PA2826283415

Gene: FGF8 HGNC NCBI

ClinVar RCV:

RCV000009695

ClinVar Variation:

9125

HGVS (amino-acid)	Matching Registered Transcripts
NP_001193318.1:p.Arg23Gly	CA254660 NM_001206389.2:c.67C>G