Canonical Allele Identifier: PA1139684792
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866141
ClinVar RCV Id: RCV001073922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Leu330dup
CA916082961
NM_000883.4:c.987_989dup