Allele Registry

Canonical Allele Identifier: PA2830102625

Gene: MID1 HGNC NCBI

ClinVar Variation Id: 92877

HGVS (amino-acid)	Matching Registered Transcripts
NP_150631.1:p.Thr625Ile	CA220693 NM_033289.2:c.1874C>T