Allele Registry

Canonical Allele Identifier: PA2825167771

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

490604

ClinVar RCV:

RCV000594239

RCV000694386

RCV002532447

ClinVar Variation:

499180

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Leu1389Pro	CA3993457 NM_000426.4:c.4166T>C