Canonical Allele Identifier: PA916072045
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 472865
ClinVar RCV Id: RCV000525236 RCV001508742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116103.1:p.Asp133Asn
CA7372293
NM_032714.3:c.397G>A