Allele Registry

Canonical Allele Identifier: PA103992

Gene: LAMB2 HGNC NCBI

ClinVar Allele:

29573

ClinVar RCV:

RCV000015633

ClinVar Variation:

14534

HGVS (amino-acid)	Matching Registered Transcripts
NP_002283.3:p.Arg246Gln	CA124112 NM_002292.4:c.737G>A