Canonical Allele Identifier: PA2825803714
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2796009
ClinVar RCV Id: RCV003667930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136048.1:p.Met122Ile
CA369174447
NM_001142576.2:c.366G>T
CA369174449
NM_001142576.2:c.366G>C
CA369174451
NM_001142576.2:c.366G>A