Allele Registry

Canonical Allele Identifier: PA2825167102

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000546757

RCV002527940

ClinVar Variation:

477448

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Asn680Ser	CA3992804 NM_000426.4:c.2039A>G