Allele Registry

Canonical Allele Identifier: PA658815847

Gene: MED25 HGNC NCBI

ClinVar RCV:

RCV000653910

RCV002264973

ClinVar Variation:

543216

HGVS (amino-acid)	Matching Registered Transcripts
NP_112235.2:p.Pro201Leu	CA9584928 NM_030973.4:c.602C>T