Allele Registry

Canonical Allele Identifier: PA2825454436

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000480247

ClinVar Variation:

422392

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Leu2814Val	CA16618243 NM_001079823.2:c.8440C>G