Canonical Allele Identifier: PA111314
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Arg214His
CA114725
NM_022489.4:c.641G>A