Canonical Allele Identifier: PA337199
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 216779
ClinVar RCV Id: RCV000197425 RCV000765458 RCV000756328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Leu480Val
CA337197
NM_030973.4:c.1438C>G