Canonical Allele Identifier: PA645503399
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 265523
ClinVar RCV Id: RCV000255571 RCV001753738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Met864Leu
CA10588542
NM_015335.5:c.2590A>T
CA386890885
NM_015335.5:c.2590A>C