Allele Registry

Canonical Allele Identifier: PA658677721

Gene: MED13L HGNC NCBI

ClinVar Variation Id: 427897

HGVS (amino-acid)	Matching Registered Transcripts
NP_056150.1:p.Asp860Gly	CA386890911 NM_015335.5:c.2579A>G