Allele Registry

Canonical Allele Identifier: PA2827407638

Gene: MID1 HGNC NCBI

ClinVar RCV:

RCV000011555

ClinVar Variation:

10808

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334662.1:p.Leu626Pro	CA255551 NM_001347733.2:c.1877T>C