Canonical Allele Identifier: PA2741950738
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 2532656
ClinVar RCV Id: RCV003253524 RCV003603155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Met902Thr
CA6811113
NM_015335.5:c.2705T>C