Canonical Allele Identifier: PA2825803283
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1488917
ClinVar RCV Id: RCV001980368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136047.1:p.Cys221Ser
CA369168699
NM_001142575.2:c.662G>C
CA369168712
NM_001142575.2:c.661T>A