Canonical Allele Identifier: PA2826173512
Gene: MID1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180206.1:p.Thr663Ile
CA220693
NM_001193277.1:c.1988C>T