Canonical Allele Identifier: PA658682362
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 449198
ClinVar RCV Id: RCV000522125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Ala525Thr
CA4470784
NM_000883.4:c.1573G>A