Allele Registry

Canonical Allele Identifier: PA2580393302

Gene: MED13L HGNC NCBI

ClinVar Allele:

2096240

ClinVar RCV:

RCV002909145

ClinVar Variation:

2046106

HGVS (amino-acid)	Matching Registered Transcripts
NP_056150.1:p.Arg1342His	CA386885347 NM_015335.5:c.4025G>A