Canonical Allele Identifier: PA2741950736
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 3062233
ClinVar RCV Id: RCV003985955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Pro869Leu
CA386890851
NM_015335.5:c.2606C>T