Canonical Allele Identifier: PA658816812
Gene: MAB21L2 HGNC NCBI

Linked Data

ClinVar Variation Id: 504384
ClinVar RCV Id: RCV000598605
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006430.1:p.Arg163_Glu164insAlaLeuIleArg
CA658796471
NM_006439.5:c.490_491insCGCTCATCAGGG