Canonical Allele Identifier: PA2827364459
Gene: FNIP1 HGNC NCBI
ClinVar RCV:
RCV002959209
ClinVar Variation:
2070880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333043.1:p.Pro1055Ser
CA3400368
NM_001346114.2:c.3163C>T