Canonical Allele Identifier: PA2827364425
Gene: FNIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2045748
ClinVar RCV Id: RCV002900600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333043.1:p.Phe839Leu
CA3400484
NM_001346114.2:c.2515T>C
CA360788668
NM_001346114.2:c.2517T>G
CA360788669
NM_001346114.2:c.2517T>A