Canonical Allele Identifier: PA645490094
Gene: IMPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 342353
ClinVar RCV Id: RCV000278383 RCV000912285 RCV003888821 RCV003950195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057331.2:p.Arg390His
CA2519255
NM_016247.4:c.1169G>A