Canonical Allele Identifier: PA658677735
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 453115
ClinVar RCV Id: RCV000522464 RCV003603057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Ala1143Val
CA6810981
NM_015335.5:c.3428C>T