Allele Registry

Canonical Allele Identifier: PA2825168226

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000078779

RCV000224783

RCV000525182

RCV000656110

RCV001152792

RCV001258302

ClinVar Variation:

92968

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Arg1844Ser	CA146139 NM_000426.4:c.5530C>A