Canonical Allele Identifier: PA2825802968
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 194714
ClinVar RCV Id: RCV000175148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136046.1:p.Arg507Trp
CA240847
NM_001142574.2:c.1519C>T