Allele Registry

Canonical Allele Identifier: PA2825168597

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000723769

RCV001080713

ClinVar Variation:

167246

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Val2233Ile	CA234205 NM_000426.4:c.6697G>A