Allele Registry

Canonical Allele Identifier: PA658675869

Gene: LAMB2 HGNC NCBI

ClinVar RCV:

RCV000544140

RCV004553240

ClinVar Variation:

472487

HGVS (amino-acid)	Matching Registered Transcripts
NP_002283.3:p.Arg156His	CA352751228 NM_002292.4:c.467G>A