Canonical Allele Identifier: PA916059086
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 653247
ClinVar RCV Id: RCV000808989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Pro206Leu
CA9584934
NM_030973.4:c.617C>T