Allele Registry

Canonical Allele Identifier: PA2573062630

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000480247

ClinVar Variation:

422392

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Leu2818Val	CA16618243 NM_000426.4:c.8452C>G