Canonical Allele Identifier: PA645490599
Gene: IMPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 342335
ClinVar RCV Id: RCV000288559 RCV002057814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057331.2:p.Ala1168Gly
CA2518734
NM_016247.4:c.3503C>G