Allele Registry

Canonical Allele Identifier: PA2580297840

Gene: FGF18 HGNC NCBI

ClinVar RCV:

RCV004156506

ClinVar Variation:

2313201

HGVS (amino-acid)	Matching Registered Transcripts
NP_003853.1:p.Pro183Leu	CA3559025 NM_003862.3:c.548C>T