Canonical Allele Identifier: PA645475861
Gene: MID2 HGNC NCBI

Linked Data

ClinVar Variation Id: 435871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036348.2:p.Arg715Gln
CA10486250
NM_012216.3:c.2144G>A