Canonical Allele Identifier: PA2828755688
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 409954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Val213Ala
CA9584944
NM_001378355.1:c.638T>C