Canonical Allele Identifier: PA2825803929
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866594
ClinVar RCV Id: RCV001074713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136048.1:p.Lys280_Lys281insPhe
CA916082962
NM_001142576.2:c.840_841insTTC