Canonical Allele Identifier: PA2741819038
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3027889
ClinVar RCV Id: RCV003891143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Gln350Lys
CA369168019
NM_000883.4:c.1048C>A