Canonical Allele Identifier: PA645489885
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312688
ClinVar RCV Id: RCV000267568 RCV000419174 RCV000860568 RCV001727680 RCV002392855
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Cys484Tyr
CA7372572
NM_022489.4:c.1451G>A