Canonical Allele Identifier: PA2825869372
Gene: IMPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1031546
ClinVar RCV Id: RCV001333408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138351.1:p.Glu127Gln
CA4792604
NM_001144879.2:c.379G>C