Canonical Allele Identifier: PA2826174047
Gene: MID1 HGNC NCBI

Linked Data

ClinVar Variation Id: 10811
ClinVar RCV Id: RCV000011558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180208.1:p.Leu295Pro
CA255555
NM_001193279.1:c.884T>C