Canonical Allele Identifier: PA916072168
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1052
ClinVar RCV Id: RCV000001107 RCV001380436 RCV003987303
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116103.1:p.Arg218Trp
CA114724
NM_032714.3:c.652C>T