Canonical Allele Identifier: PA2825803259
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 254167
ClinVar RCV Id: RCV000240659
ClinVar Variation Id: 1388602
ClinVar RCV Id: RCV001908409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Gln218His
CA10586358
NM_001142575.2:c.654G>C
CA369168756
NM_001142575.2:c.654G>T