Canonical Allele Identifier: PA2580393272
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 1803299
ClinVar RCV Id: RCV002466969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Asp1151Asn
CA386887713
NM_015335.5:c.3451G>A