Canonical Allele Identifier: PA1139747182
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 995689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Gln310His
CA406914854
NM_030973.4:c.930A>T
CA406914856
NM_030973.4:c.930A>C