Canonical Allele Identifier: PA2825548438
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866656
ClinVar RCV Id: RCV001074851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001096075.1:p.Asn305Tyr
CA369169260
NM_001102605.2:c.913A>T