Allele Registry

Canonical Allele Identifier: PA915967184

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000413698

RCV000557605

RCV000764623

RCV001252052

RCV001508557

RCV002523936

ClinVar Variation:

373189

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.His1082Tyr	CA3993219 NM_001079823.2:c.3244C>T