Allele Registry

Canonical Allele Identifier: PA103999

Gene: LAMB2 HGNC NCBI

ClinVar RCV:

RCV000015629

RCV001335017

RCV001849266

RCV002504793

ClinVar Variation:

14530

HGVS (amino-acid)	Matching Registered Transcripts
NP_002283.3:p.Arg246Trp	CA124107 NM_002292.4:c.736C>T