Canonical Allele Identifier: PA645379801
Gene: AGPAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 259977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006403.2:p.Leu17dup
CA2692655378
NM_006412.4:c.51_52insTTG
CA2692655379
NM_006412.4:c.48_49insTTG
CA2692655380
NM_006412.4:c.47_48insACT
CA2692655381
NM_006412.4:c.45_46insTTG
CA2720909497
NM_006412.4:c.50_51insTCT
CA2720909530
NM_006412.4:c.50_51insCCT
CA2720909548
NM_006412.4:c.47_48insTCT
CA2720909625
NM_006412.4:c.44_45insTCT
CA2720909640
NM_006412.4:c.44_45insACT