Canonical Allele Identifier: PA915981022
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 642813
ClinVar RCV Id: RCV000796350
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Arg420Ser
CA386898212
NM_015335.5:c.1260A>T
CA386898213
NM_015335.5:c.1260A>C