Canonical Allele Identifier: PA2741950860
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 3025773
ClinVar RCV Id: RCV003885161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Pro2183Leu
CA6810335
NM_015335.5:c.6548C>T