Canonical Allele Identifier: PA220694
Gene: MID1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000372.1:p.Thr663Ile
CA220693
NM_000381.4:c.1988C>T