Canonical Allele Identifier: PA2580506605
Gene: FNIP1 HGNC NCBI
ClinVar RCV:
RCV003024651
ClinVar Variation:
2116300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_588613.3:p.Pro822Leu
CA360789878
NM_133372.3:c.2465C>T