Canonical Allele Identifier: PA097738
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 2108
ClinVar RCV Id: RCV000002189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Asp2023Gly
CA115348
NM_015335.5:c.6068A>G