Canonical Allele Identifier: PA2580266725
Gene: MGAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1951756
ClinVar RCV Id: RCV002695113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002399.1:p.Phe272Leu
CA389620582
NM_002408.4:c.814T>C
CA389620592
NM_002408.4:c.816C>A
CA389620593
NM_002408.4:c.816C>G