Canonical Allele Identifier: PA2825351921
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312704
ClinVar RCV Id: RCV000269885 RCV000691072
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Thr996Ile
CA7373144
NM_001031714.3:c.2987C>T