Canonical Allele Identifier: PA2580393130
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 2145137
ClinVar RCV Id: RCV003064876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Cys165Tyr
CA386872529
NM_015335.5:c.494G>A