Canonical Allele Identifier: PA236193
Gene: IMPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 191179
ClinVar RCV Id: RCV000171365 RCV000987301 RCV000958677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057331.2:p.Pro1147Ser
CA236192
NM_016247.4:c.3439C>T