Canonical Allele Identifier: PA2573293095
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1487843
ClinVar RCV Id: RCV002008879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116103.1:p.Gly63Asp
CA267330439
NM_032714.3:c.188G>A