Canonical Allele Identifier: PA2573262616
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 1404911
ClinVar RCV Id: RCV001899129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Val1119Met
CA244149957
NM_015335.5:c.3355G>A