Canonical Allele Identifier: PA645455157
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 329887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Pro656Thr
CA9585443
NM_030973.4:c.1966C>A