Canonical Allele Identifier: PA2827364409
Gene: FNIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2116300
ClinVar RCV Id: RCV003024651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333043.1:p.Pro777Leu
CA360789878
NM_001346114.2:c.2330C>T