Canonical Allele Identifier: PA124388
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14838
ClinVar RCV Id: RCV000015963
ClinVar Variation Id: 1457411
ClinVar RCV Id: RCV001972635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001096075.1:p.Asn273Lys
CA124382
NM_001102605.2:c.819T>G
CA369171839
NM_001102605.2:c.819T>A