Canonical Allele Identifier: PA2826894515
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2849769
ClinVar RCV Id: RCV003687975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291450.1:p.Leu261Val
CA369168737
NM_001304521.2:c.781C>G
CA2739278929
NM_001304521.2:c.780_781delinsCG