Canonical Allele Identifier: PA645490202
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312700
ClinVar RCV Id: RCV000301022 RCV000527454 RCV001508744 RCV002418164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Ile685Val
CA7372814
NM_022489.4:c.2053A>G