Canonical Allele Identifier: PA174622
Gene: IMPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161700
ClinVar RCV Id: RCV000149236 RCV002514862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057331.2:p.Pro422Leu
CA174621
NM_016247.4:c.1265C>T