Canonical Allele Identifier: PA2828755696
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 574168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Val227Met
CA9584954
NM_001378355.1:c.679G>A