Canonical Allele Identifier: PA2828755645
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 183670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Arg140Trp
CA235584
NM_001378355.1:c.418C>T