Canonical Allele Identifier: PA2741999596
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2943595
ClinVar RCV Id: RCV003803153
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116103.1:p.Ala213Glu
CA391213428
NM_032714.3:c.638C>A