Allele Registry

Canonical Allele Identifier: PA915967641

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000284205

RCV000536495

RCV000712196

RCV000764631

RCV001293062

RCV003992282

ClinVar Variation:

355294

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Arg2353Cys	CA3994427 NM_001079823.2:c.7057C>T