Canonical Allele Identifier: PA2825350826
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1051
ClinVar RCV Id: RCV000001106 RCV000681691 RCV001239762 RCV002293970 RCV003352745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Arg218Gln
CA114723
NM_001031714.3:c.653G>A