Allele Registry

Canonical Allele Identifier: PA915967324

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

490604

ClinVar RCV:

RCV000594239

RCV000694386

RCV002532447

ClinVar Variation:

499180

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Leu1389Pro	CA3993457 NM_001079823.2:c.4166T>C