Canonical Allele Identifier: PA2573172902
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1380019
ClinVar RCV Id: RCV001917109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Asp301Gly
CA369169685
NM_000883.4:c.902A>G