Canonical Allele Identifier: PA097725
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 2107
ClinVar RCV Id: RCV000002188
JSON-LD

Amino-acid Alleles

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