Canonical Allele Identifier: PA2825293666
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_001008738.3:p.Asp876Glu
CA3400473
NM_001008738.3:c.2628C>G
CA360788289
NM_001008738.3:c.2628C>A