Canonical Allele Identifier: PA2825803974
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2849769
ClinVar RCV Id: RCV003687975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136048.1:p.Leu297Val
CA369168737
NM_001142576.2:c.889C>G
CA2739278929
NM_001142576.2:c.888_889delinsCG