Allele Registry

Canonical Allele Identifier: PA2580393383

Gene: MED13L HGNC NCBI

ClinVar RCV:

RCV002290942

ClinVar Variation:

1708633

HGVS (amino-acid)	Matching Registered Transcripts
NP_056150.1:p.Arg1872Pro	CA386878621 NM_015335.5:c.5615G>C