Canonical Allele Identifier: PA111413
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30868
ClinVar RCV Id: RCV000023853
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Leu132Arg
CA129513
NM_022489.4:c.395T>G