Canonical Allele Identifier: PA2825350631
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30868
ClinVar RCV Id: RCV000023853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Leu132Arg
CA129513
NM_001031714.3:c.395T>G