Canonical Allele Identifier: PA658677747
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 450904
ClinVar RCV Id: RCV000522127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Gln1725His
CA386880941
NM_015335.5:c.5175G>C
CA386880942
NM_015335.5:c.5175G>T