Canonical Allele Identifier: PA2741950854
Gene: MED13L HGNC NCBI
ClinVar RCV:
RCV003499640
ClinVar Variation:
2725912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Val2101Ile
CA6810402
NM_015335.5:c.6301G>A