Canonical Allele Identifier: PA2825293697
Gene: FNIP1 HGNC NCBI
ClinVar RCV:
RCV002959209
ClinVar Variation:
2070880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008738.3:p.Pro1072Ser
CA3400368
NM_001008738.3:c.3214C>T