Canonical Allele Identifier: PA148794
Gene: IMPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95749
ClinVar RCV Id: RCV000081792 RCV000401059 RCV000898540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057331.2:p.Pro1013Leu
CA148793
NM_016247.4:c.3038C>T