Canonical Allele Identifier: PA2828755670
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 619180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Arg186Trp
CA9584913
NM_001378355.1:c.556C>T