Canonical Allele Identifier: PA645490097
Gene: IMPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 342352
ClinVar RCV Id: RCV000375226 RCV000949263 RCV001000670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057331.2:p.Thr408Met
CA2519247
NM_016247.4:c.1223C>T