Canonical Allele Identifier: PA891850704
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 574168
ClinVar RCV Id: RCV000696026 RCV002264978 RCV003163200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Val227Met
CA9584954
NM_030973.4:c.679G>A