Canonical Allele Identifier: PA916050780
Gene: MID2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143857
ClinVar RCV Id: RCV000133396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_438112.2:p.Arg347Gln
CA170511
NM_052817.3:c.1040G>A