Canonical Allele Identifier: PA2828755969
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 329887
ClinVar RCV Id: RCV000532947 RCV000996970 RCV001172666 RCV001822857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Pro656Thr
CA9585443
NM_001378355.1:c.1966C>A