Canonical Allele Identifier: PA1139747091
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 839297
ClinVar RCV Id: RCV001041019 RCV002551484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Arg192Trp
CA9584918
NM_030973.4:c.574C>T