Canonical Allele Identifier: PA2828755669
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 917361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Arg186Gln
CA406912980
NM_001378355.1:c.557G>A