Allele Registry

Canonical Allele Identifier: PA2580506629

Gene: FNIP1 HGNC NCBI

ClinVar RCV:

RCV002999196

RCV002999197

ClinVar Variation:

2082517

HGVS (amino-acid)	Matching Registered Transcripts
NP_588613.3:p.His1106Arg	CA3400353 NM_133372.3:c.3317A>G