Canonical Allele Identifier: PA645415557
Gene: MED12 HGNC NCBI
ClinVar RCV:
RCV000496123
ClinVar Variation:
431098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005111.2:p.Ser849Pro
CA413515683
NM_005120.3:c.2545T>C