Canonical Allele Identifier: PA235586
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 183670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Arg140Trp
CA235584
NM_030973.4:c.418C>T