Canonical Allele Identifier: PA2825803957
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371890
ClinVar RCV Id: RCV001879212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136048.1:p.Lys290Asn
CA369168984
NM_001142576.2:c.870G>T
CA369168990
NM_001142576.2:c.870G>C