Canonical Allele Identifier: PA2828755683
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 653247
ClinVar RCV Id: RCV000808989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Pro206Leu
CA9584934
NM_001378355.1:c.617C>T