Canonical Allele Identifier: PA2825802628
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 254167
ClinVar RCV Id: RCV000240659
ClinVar Variation Id: 1388602
ClinVar RCV Id: RCV001908409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136046.1:p.Gln238His
CA10586358
NM_001142574.2:c.714G>C
CA369168756
NM_001142574.2:c.714G>T