Canonical Allele Identifier: PA645376477
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 254167
ClinVar RCV Id: RCV000240659
ClinVar Variation Id: 1388602
ClinVar RCV Id: RCV001908409
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Gln328His
CA10586358
NM_000883.4:c.984G>C
CA369168756
NM_000883.4:c.984G>T