Allele Registry

Canonical Allele Identifier: PA2825168152

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

425661

ClinVar RCV:

RCV000689906

RCV000712189

RCV003302734

ClinVar Variation:

432756

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Glu1764Gly	CA3993839 NM_000426.4:c.5291A>G