Canonical Allele Identifier: PA1139684789
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 937932
ClinVar RCV Id: RCV001207064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Lys323Arg
CA369169029
NM_000883.4:c.968A>G