Canonical Allele Identifier: PA658815353
Gene: MGAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 530392
ClinVar RCV Id: RCV000636242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002399.1:p.Thr230Pro
CA389619912
NM_002408.4:c.688A>C