Canonical Allele Identifier: PA2825211522
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2796009
ClinVar RCV Id: RCV003667930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Met155Ile
CA369174447
NM_000883.4:c.465G>T
CA369174449
NM_000883.4:c.465G>C
CA369174451
NM_000883.4:c.465G>A