Canonical Allele Identifier: PA645490128
Gene: IMPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 342350
ClinVar RCV Id: RCV000389498 RCV000980050 RCV003972442 RCV003888820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057331.2:p.Thr461Arg
CA2519176
NM_016247.4:c.1382C>G