Allele Registry

Canonical Allele Identifier: PA2580297832

Gene: FGF18 HGNC NCBI

ClinVar RCV:

RCV004150509

ClinVar Variation:

2302652

HGVS (amino-acid)	Matching Registered Transcripts
NP_003853.1:p.Pro5Ser	CA362137983 NM_003862.3:c.13C>T