Canonical Allele Identifier: PA2741950759
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 2700568
ClinVar RCV Id: RCV003498229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Leu1115Ile
CA386888090
NM_015335.5:c.3343C>A