Canonical Allele Identifier: PA1139747047
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 932437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Arg176Trp
CA9584904
NM_030973.4:c.526C>T