Canonical Allele Identifier: PA2580393140
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 2169893
ClinVar RCV Id: RCV003085060
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Pro204Leu
CA6811633
NM_015335.5:c.611C>T