Canonical Allele Identifier: PA2825350488
Gene: INF2 HGNC NCBI
ClinVar RCV:
RCV001866370
ClinVar Variation:
1354336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Gly88Cys
CA391225673
NM_001031714.3:c.262G>T