Canonical Allele Identifier: PA891850702
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 576913
ClinVar RCV Id: RCV000699542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Ile182Val
CA406912937
NM_030973.4:c.544A>G