Canonical Allele Identifier: PA2825802579
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 374177
ClinVar RCV Id: RCV000415244 RCV001198950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136046.1:p.Thr220Pro
CA16043423
NM_001142574.2:c.658A>C