Canonical Allele Identifier: PA2580393266
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 2231958
ClinVar RCV Id: RCV002723024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Thr1077Ala
CA386888617
NM_015335.5:c.3229A>G