Canonical Allele Identifier: PA2825801963
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1513705
ClinVar RCV Id: RCV002026303 RCV003303647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136045.1:p.Tyr233His
CA369169194
NM_001142573.2:c.697T>C