Canonical Allele Identifier: PA2741913766
Gene: MED12 HGNC NCBI
ClinVar RCV:
RCV003763555
ClinVar Variation:
2882760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005111.2:p.Pro1408Leu
CA413525915
NM_005120.3:c.4223C>T