Canonical Allele Identifier: PA645455143
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 409954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Val213Ala
CA9584944
NM_030973.4:c.638T>C