Allele Registry

Canonical Allele Identifier: PA2825454089

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000698683

ClinVar Variation:

576235

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Arg2574Gly	CA365628402 NM_001079823.2:c.7720C>G