Canonical Allele Identifier: PA2825803971
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866141
ClinVar RCV Id: RCV001073922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136048.1:p.Leu297dup
CA916082961
NM_001142576.2:c.888_890dup