Canonical Allele Identifier: PA124389
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14838
ClinVar RCV Id: RCV000015963
ClinVar Variation Id: 1457411
ClinVar RCV Id: RCV001972635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Asn283Lys
CA124382
NM_000883.4:c.849T>G
CA369171839
NM_000883.4:c.849T>A