Canonical Allele Identifier: PA160390
Gene: MED12 HGNC NCBI

Linked Data

ClinVar Variation Id: 134636
ClinVar RCV Id: RCV000121329 RCV000228384 RCV001697144 RCV002321600 RCV002492431 RCV003985274 RCV003595865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005111.2:p.Pro1371Ser
CA160389
NM_005120.3:c.4111C>T