Canonical Allele Identifier: PA913200331
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 619180
ClinVar RCV Id: RCV000758140 RCV001174290 RCV002274097 RCV002533814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Arg186Trp
CA9584913
NM_030973.4:c.556C>T