Canonical Allele Identifier: PA2825352054
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 472851
ClinVar RCV Id: RCV000526867 RCV002448771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Arg1075His
CA7373207
NM_001031714.3:c.3224G>A