Allele Registry

Canonical Allele Identifier: PA645376477

Gene: IMPDH1 HGNC NCBI

ClinVar RCV:

RCV000240659

RCV001908409

ClinVar Variation:

254167

1388602

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