Canonical Allele Identifier: PA2741950854
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 2725912
ClinVar RCV Id: RCV003499640
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Val2101Ile
CA6810402
NM_015335.5:c.6301G>A