Canonical Allele Identifier: PA2499239715
Gene: IMPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1029977
ClinVar RCV Id: RCV001331415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138350.1:p.Gly299Asp
CA371580561
NM_001144878.2:c.896G>A