Canonical Allele Identifier: PA2580506628
Gene: FNIP1 HGNC NCBI
ClinVar RCV:
RCV002959209
ClinVar Variation:
2070880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_588613.3:p.Pro1100Ser
CA3400368
NM_133372.3:c.3298C>T