Canonical Allele Identifier: PA2499239713
Gene: IMPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1031546
ClinVar RCV Id: RCV001333408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138350.1:p.Glu186Gln
CA4792604
NM_001144878.2:c.556G>C