Canonical Allele Identifier: PA1139747096
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 947533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Pro210Leu
CA9584939
NM_030973.4:c.629C>T