Canonical Allele Identifier: PA2826894490
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14834
ClinVar RCV Id: RCV000015959 RCV000255540 RCV003887871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Asp242Asn
CA257369
NM_001304521.2:c.724G>A