Allele Registry

Canonical Allele Identifier: PA658675905

Gene: LAMB2 HGNC NCBI

ClinVar RCV:

RCV000548194

RCV001149697

RCV001149698

ClinVar Variation:

472477

HGVS (amino-acid)	Matching Registered Transcripts
NP_002283.3:p.Ile1183Val	CA2394016 NM_002292.4:c.3547A>G