Canonical Allele Identifier: PA2826894657
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 358871
ClinVar RCV Id: RCV000308314 RCV000395963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Met499Ile
CA10628265
NM_001304521.2:c.1497G>A
CA369161819
NM_001304521.2:c.1497G>T
CA369161822
NM_001304521.2:c.1497G>C