Canonical Allele Identifier: PA658678425
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 476808
ClinVar RCV Id: RCV000559469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Met220Leu
CA309515593
NM_030973.4:c.658A>T
CA406913458
NM_030973.4:c.658A>C