Canonical Allele Identifier: PA2830411537
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371890
ClinVar RCV Id: RCV001879212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899066.1:p.Lys287Asn
CA369168984
NM_183243.3:c.861G>T
CA369168990
NM_183243.3:c.861G>C