Allele Registry

Canonical Allele Identifier: PA891854527

Gene: LAMB2 HGNC NCBI

ClinVar Variation Id: 586112

HGVS (amino-acid)	Matching Registered Transcripts
NP_002283.3:p.Thr890Ile	CA2394255 NM_002292.4:c.2669C>T