Allele Registry

Canonical Allele Identifier: PA2825166965

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

98847

ClinVar RCV:

RCV000078749

RCV000428463

RCV001081152

RCV001157937

RCV002514385

RCV004528282

ClinVar Variation:

92940

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Leu545Gln	CA146102 NM_000426.4:c.1634T>A