Allele Registry

Canonical Allele Identifier: PA2825454910

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

267776

ClinVar RCV:

RCV000725292

RCV001085018

RCV001155234

ClinVar Variation:

283539

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Val3110Ile	CA3995105 NM_001079823.2:c.9328G>A