Canonical Allele Identifier: PA2828755692
Gene: MED25 HGNC NCBI

Linked Data

ClinVar Variation Id: 476808
ClinVar RCV Id: RCV000559469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365284.1:p.Met220Leu
CA309515593
NM_001378355.1:c.658A>T
CA406913458
NM_001378355.1:c.658A>C