Allele Registry

Canonical Allele Identifier: PA104034

Gene: LAMB2 HGNC NCBI

ClinVar RCV:

RCV000022640

RCV002482898

ClinVar Variation:

29774

HGVS (amino-acid)	Matching Registered Transcripts
NP_002283.3:p.His147Arg	CA128633 NM_002292.4:c.440A>G