Canonical Allele Identifier: PA2830130606
Gene: MID2 HGNC NCBI

Linked Data

ClinVar Variation Id: 435871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_438112.2:p.Arg685Gln
CA10486250
NM_052817.3:c.2054G>A