Canonical Allele Identifier: PA658677736
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 464490
ClinVar RCV Id: RCV000543892 RCV002526114 RCV004537968 RCV000763795
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Gly1173Ser
CA6810974
NM_015335.5:c.3517G>A