Canonical Allele Identifier: PA645376460
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 358878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Thr257Ala
CA4471065
NM_000883.4:c.769A>G