Canonical Allele Identifier: PA916072156
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1053
ClinVar RCV Id: RCV000001108 RCV001380435 RCV002293971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116103.1:p.Arg214His
CA114725
NM_032714.3:c.641G>A