Canonical Allele Identifier: PA109387
Gene: AGPAT2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006403.2:p.Leu228Pro
CA277946
NM_006412.4:c.683T>C