Canonical Allele Identifier: PA221942
Gene: MGAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 94062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002399.1:p.Val245Leu
CA221941
NM_002408.4:c.733G>C
CA389620190
NM_002408.4:c.733G>T