Canonical Allele Identifier: PA645509688
Gene: IMPG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 438085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001554.2:p.Ala386Asp
CA3898212
NM_001563.4:c.1157C>A