Canonical Allele Identifier: PA2825293697
Gene: FNIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2070880
ClinVar RCV Id: RCV002959209
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008738.3:p.Pro1072Ser
CA3400368
NM_001008738.3:c.3214C>T