Canonical Allele Identifier: PA658815847
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 543216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Pro201Leu
CA9584928
NM_030973.4:c.602C>T