Canonical Allele Identifier: PA2828755681
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 543216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Pro201Leu
CA9584928
NM_001378355.1:c.602C>T