Canonical Allele Identifier: PA2741913766
Gene: MED12 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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