Allele Registry

Canonical Allele Identifier: PA104025

Gene: LAMB2 HGNC NCBI

ClinVar RCV:

RCV000015635

ClinVar Variation:

14536

HGVS (amino-acid)	Matching Registered Transcripts
NP_002283.3:p.Cys321Arg	CA124113 NM_002292.4:c.961T>C