Canonical Allele Identifier: PA2830102629
Gene: MID1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_150631.1:p.Pro629Leu
CA146060
NM_033289.2:c.1886C>T