Canonical Allele Identifier: PA2825548422
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 956524
ClinVar RCV Id: RCV001229348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001096075.1:p.Asp291Asn
CA4470989
NM_001102605.2:c.871G>A