Allele Registry

Canonical Allele Identifier: PA2830102595

Gene: MID1 HGNC NCBI

ClinVar RCV:

RCV000011555

ClinVar Variation:

10808

HGVS (amino-acid)	Matching Registered Transcripts
NP_150631.1:p.Leu588Pro	CA255551 NM_033289.2:c.1763T>C