Canonical Allele Identifier: PA645376494
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 358871
ClinVar RCV Id: RCV000308314 RCV000395963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Met568Ile
CA10628265
NM_000883.4:c.1704G>A
CA369161819
NM_000883.4:c.1704G>T
CA369161822
NM_000883.4:c.1704G>C