Canonical Allele Identifier: PA093636
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 1324
ClinVar RCV Id: RCV000001387 RCV000192241 RCV000416086 RCV001082848 RCV001262290 RCV002227925 RCV001818117 RCV003924791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112235.2:p.Ala335Val
CA248234
NM_030973.4:c.1004C>T