Canonical Allele Identifier: PA257392
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Arg309Pro
CA257385
NM_000883.4:c.926G>C