Canonical Allele Identifier: PA1139684782
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 931699
ClinVar RCV Id: RCV001198547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Lys323Thr
CA369169020
NM_000883.4:c.968A>C