Allele Registry

Canonical Allele Identifier: PA645485349

Gene: LAMB2 HGNC NCBI

ClinVar RCV:

RCV000271632

RCV000366666

RCV001516710

RCV001753813

RCV003922518

ClinVar Variation:

346014

HGVS (amino-acid)	Matching Registered Transcripts
NP_002283.3:p.Ala34Asp	CA2395047 NM_002292.4:c.101C>A