Canonical Allele Identifier: PA2828755734
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 1480554
ClinVar RCV Id: RCV001993965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Gln282His
CA9585052
NM_001378355.1:c.846G>C
CA9585053
NM_001378355.1:c.846G>T