Canonical Allele Identifier: PA2741950796
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 2634411
ClinVar RCV Id: RCV004531710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Leu1460Pro
CA386883768
NM_015335.5:c.4379T>C