Allele Registry

Canonical Allele Identifier: PA2830099900

Gene: FGF8 HGNC NCBI

ClinVar RCV:

RCV000009695

ClinVar Variation:

9125

HGVS (amino-acid)	Matching Registered Transcripts
NP_149355.1:p.Arg87Gly	CA254660 NM_033165.4:c.259C>G