Canonical Allele Identifier: PA916072165
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1051
ClinVar RCV Id: RCV000001106 RCV000681691 RCV001239762 RCV002293970 RCV003352745
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116103.1:p.Arg218Gln
CA114723
NM_032714.3:c.653G>A