Canonical Allele Identifier: PA2828755732
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 2153255
ClinVar RCV Id: RCV003077517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Ser279Asn
CA9585051
NM_001378355.1:c.836G>A