Canonical Allele Identifier: PA2828755750
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 995689
ClinVar RCV Id: RCV001289860 RCV001859228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Gln310His
CA406914854
NM_001378355.1:c.930A>T
CA406914856
NM_001378355.1:c.930A>C