Canonical Allele Identifier: PA2573172922
Gene: IMPDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371890
ClinVar RCV Id: RCV001879212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000874.2:p.Lys323Asn
CA369168984
NM_000883.4:c.969G>T
CA369168990
NM_000883.4:c.969G>C