Allele Registry

Canonical Allele Identifier: PA2825293662

Gene: FNIP1 HGNC NCBI

ClinVar RCV:

RCV002900600

ClinVar Variation:

2045748

HGVS (amino-acid)	Matching Registered Transcripts
NP_001008738.3:p.Phe856Leu	CA3400484 NM_001008738.3:c.2566T>C CA360788668 NM_001008738.3:c.2568T>G CA360788669 NM_001008738.3:c.2568T>A