Canonical Allele Identifier: PA2825293646
Gene: FNIP1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008738.3:p.Pro794Leu
CA360789878
NM_001008738.3:c.2381C>T