Allele Registry

Canonical Allele Identifier: PA097725

Gene: MED13L HGNC NCBI

ClinVar RCV:

RCV000002188

ClinVar Variation:

2107

HGVS (amino-acid)	Matching Registered Transcripts
NP_056150.1:p.Arg1872His	CA115347 NM_015335.5:c.5615G>A