Canonical Allele Identifier: PA2828755619
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 421749
ClinVar RCV Id: RCV000482797 RCV001238346 RCV001249635 RCV003319988
ClinVar Variation Id: 2805655
ClinVar RCV Id: RCV003745955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Gly106Arg
CA9584809
NM_001378355.1:c.316G>A
CA406911931
NM_001378355.1:c.316G>C