Allele Registry

Canonical Allele Identifier: PA118873

Gene: FGF10 HGNC NCBI

ClinVar RCV:

RCV000007970

RCV000659642

ClinVar Variation:

7534

HGVS (amino-acid)	Matching Registered Transcripts
NP_004456.1:p.Arg80Ser	CA118872 NM_004465.2:c.240A>C CA359699348 NM_004465.2:c.240A>T