Allele Registry

Canonical Allele Identifier: PA2825168208

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

456102

ClinVar RCV:

RCV000526524

RCV003133366

ClinVar Variation:

477489

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Gly1824Ser	CA3993892 NM_000426.4:c.5470G>A