Allele Registry

Canonical Allele Identifier: PA2580506611

Gene: FNIP1 HGNC NCBI

ClinVar RCV:

RCV002900600

ClinVar Variation:

2045748

HGVS (amino-acid)	Matching Registered Transcripts
NP_588613.3:p.Phe884Leu	CA3400484 NM_133372.3:c.2650T>C CA360788668 NM_133372.3:c.2652T>G CA360788669 NM_133372.3:c.2652T>A