Allele Registry

Canonical Allele Identifier: PA2741950759

Gene: MED13L HGNC NCBI

ClinVar Allele:

2855567

ClinVar RCV:

RCV003498229

ClinVar Variation:

2700568

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