Canonical Allele Identifier: PA2827364429
Gene: FNIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2042018
ClinVar RCV Id: RCV002917160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333043.1:p.Asp859Glu
CA3400473
NM_001346114.2:c.2577C>G
CA360788289
NM_001346114.2:c.2577C>A