Canonical Allele Identifier: PA1139684714
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 931488
ClinVar RCV Id: RCV001198071
ClinVar Variation Id: 1810221
ClinVar RCV Id: RCV002508869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Lys314Asn
CA369169270
NM_000883.4:c.942G>T
CA369169283
NM_000883.4:c.942G>C