Canonical Allele Identifier: PA1139721246
Gene: MED13L HGNC NCBI

Linked Data

ClinVar Variation Id: 835348
ClinVar RCV Id: RCV001036208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056150.1:p.Gln201His
CA386872155
NM_015335.5:c.603G>T
CA386872156
NM_015335.5:c.603G>C