Allele Registry

Canonical Allele Identifier: PA2825167490

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000413698

RCV000557605

RCV000764623

RCV001252052

RCV001508557

RCV002523936

ClinVar Variation:

373189

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.His1082Tyr	CA3993219 NM_000426.4:c.3244C>T