Canonical Allele Identifier: PA2827407663
Gene: MID1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334662.1:p.Pro667Leu
CA146060
NM_001347733.2:c.2000C>T