Canonical Allele Identifier: PA658654371
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_057063.2:p.Ile812Thr
CA365668461
NM_015979.4:c.2435T>C