Canonical Allele Identifier: PA249932
Gene: MGAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30270

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002399.1:p.Lys237Asn
CA249931
NM_002408.4:c.711G>C
CA389620059
NM_002408.4:c.711G>T