Canonical Allele Identifier: PA1139684687
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 956524
ClinVar RCV Id: RCV001229348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Asp301Asn
CA4470989
NM_000883.4:c.901G>A