Canonical Allele Identifier: PA257382
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14835
ClinVar RCV Id: RCV000015960 RCV002513068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136048.1:p.Val320Ile
CA257377
NM_001142576.2:c.958G>A