Canonical Allele Identifier: PA916005850
Gene: RIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 425267
ClinVar RCV Id: RCV000487574 RCV002525998 RCV003932790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229510.1:p.Ile925Thr
CA9780339
NM_001242581.2:c.2774T>C