Canonical Allele Identifier: PA2580393269
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 2159042
ClinVar RCV Id: RCV003072609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Ala1098Thr
CA6810998
NM_015335.5:c.3292G>A