Canonical Allele Identifier: PA645490176
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312696
ClinVar RCV Id: RCV000389255 RCV002522296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Arg622Gln
CA7372693
NM_022489.4:c.1865G>A