Canonical Allele Identifier: PA2825802647
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1488917
ClinVar RCV Id: RCV001980368
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136046.1:p.Cys241Ser
CA369168699
NM_001142574.2:c.722G>C
CA369168712
NM_001142574.2:c.721T>A