Canonical Allele Identifier: PA2825803917
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2735088
ClinVar RCV Id: RCV003555371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136048.1:p.Leu279Pro
CA369169375
NM_001142576.2:c.836T>C