Canonical Allele Identifier: PA2580393240
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 2319866
ClinVar RCV Id: RCV002905927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Val892Leu
CA386890693
NM_015335.5:c.2674G>T
CA386890694
NM_015335.5:c.2674G>C