Canonical Allele Identifier: PA916059079
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 650610
ClinVar RCV Id: RCV000805787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Pro201Ala
CA9584927
NM_030973.4:c.601C>G