Allele Registry

Canonical Allele Identifier: PA2828755891

Gene: MED25 HGNC NCBI

ClinVar RCV:

RCV000531602

RCV000539627

RCV001174294

RCV002045152

ClinVar Variation:

476801

476802

1502368

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365284.1:p.Met559Ile	CA9585344 NM_001378355.1:c.1677G>C CA406919381 NM_001378355.1:c.1677G>T CA406919383 NM_001378355.1:c.1677G>A