Allele Registry

Canonical Allele Identifier: PA235586

Gene: MED25 HGNC NCBI

ClinVar Allele:

181570

ClinVar RCV:

RCV000162327

RCV000689030

RCV002247562

ClinVar Variation:

183670

HGVS (amino-acid)	Matching Registered Transcripts
NP_112235.2:p.Arg140Trp	CA235584 NM_030973.4:c.418C>T