Canonical Allele Identifier: PA2830411514
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866594
ClinVar RCV Id: RCV001074713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899066.1:p.Lys277_Lys278insPhe
CA916082962
NM_183243.3:c.831_832insTTC