Canonical Allele Identifier: PA2825802052
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 193819
ClinVar RCV Id: RCV000174020 RCV000322287 RCV000281510 RCV000765929 RCV000877998 RCV004535194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136045.1:p.Ala285Thr
CA239483
NM_001142573.2:c.853G>A