Canonical Allele Identifier: PA2825548457
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3109565
ClinVar RCV Id: RCV004397911
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001096075.1:p.Thr327Ser
CA369168500
NM_001102605.2:c.980C>G
CA369168504
NM_001102605.2:c.979A>T