Canonical Allele Identifier: PA2826523181
Gene: MED23 HGNC NCBI

Linked Data

ClinVar Variation Id: 441025
ClinVar RCV Id: RCV000509436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257450.1:p.Ile806Thr
CA365668461
NM_001270521.2:c.2417T>C