Canonical Allele Identifier: PA2825803977
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3109565
ClinVar RCV Id: RCV004397911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136048.1:p.Thr304Ser
CA369168500
NM_001142576.2:c.911C>G
CA369168504
NM_001142576.2:c.910A>T