Canonical Allele Identifier: PA2825293698
Gene: FNIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2082517
ClinVar RCV Id: RCV002999197 RCV002999196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008738.3:p.His1078Arg
CA3400353
NM_001008738.3:c.3233A>G