Canonical Allele Identifier: PA146061
Gene: MID1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000372.1:p.Pro667Leu
CA146060
NM_000381.4:c.2000C>T