Canonical Allele Identifier: PA2825804170
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_001136048.1:p.Ala492Thr
CA4470784
NM_001142576.2:c.1474G>A