Canonical Allele Identifier: PA658675561
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_071934.3:p.Asp133Asn
CA7372293
NM_022489.4:c.397G>A