Canonical Allele Identifier: PA2573293099
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1354336
ClinVar RCV Id: RCV001866370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116103.1:p.Gly88Cys
CA391225673
NM_032714.3:c.262G>T