Allele Registry

Canonical Allele Identifier: PA658678437

Gene: MED25 HGNC NCBI

ClinVar RCV:

RCV000531602

RCV000539627

RCV001174294

RCV002045152

ClinVar Variation:

476801

476802

1502368

HGVS (amino-acid)	Matching Registered Transcripts
NP_112235.2:p.Met559Ile	CA9585344 NM_030973.4:c.1677G>C CA406919381 NM_030973.4:c.1677G>T CA406919383 NM_030973.4:c.1677G>A