Canonical Allele Identifier: PA2741950662
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 2643371
ClinVar RCV Id: RCV003390311 RCV004364507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Gln201Glu
CA386872161
NM_015335.5:c.601C>G