Canonical Allele Identifier: PA2825293634
Gene: FNIP1 HGNC NCBI
ClinVar RCV:
RCV002639353
ClinVar Variation:
1940477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008738.3:p.Glu758Lys
CA360790255
NM_001008738.3:c.2272G>A