Canonical Allele Identifier: PA2827364425
Gene: FNIP1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333043.1:p.Phe839Leu
CA3400484
NM_001346114.2:c.2515T>C
CA360788668
NM_001346114.2:c.2517T>G
CA360788669
NM_001346114.2:c.2517T>A