Canonical Allele Identifier: PA658675630
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 450497
ClinVar RCV Id: RCV000523280 RCV001857976
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Asn1119Thr
CA7373231
NM_022489.4:c.3356A>C