Canonical Allele Identifier: PA645490416
Gene: IMPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 342345
ClinVar RCV Id: RCV000302368 RCV001058248 RCV003888819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057331.2:p.Ser811Ala
CA2518978
NM_016247.4:c.2431T>G