Canonical Allele Identifier: PA2829353222
Gene: MGAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3125902
ClinVar RCV Id: RCV004417222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002399.1:p.Asp136Val
CA7172541
NM_002408.4:c.407A>T