Canonical Allele Identifier: PA1139721458
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 978840
ClinVar RCV Id: RCV001266282 RCV001257599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Pro869Ser
CA386890852
NM_015335.5:c.2605C>T