Canonical Allele Identifier: PA2828755674
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 839297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Arg192Trp
CA9584918
NM_001378355.1:c.574C>T