Allele Registry

Canonical Allele Identifier: PA915967170

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

443878

ClinVar RCV:

RCV000522346

RCV000689663

RCV004541633

ClinVar Variation:

451960

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Ser1052Gly	CA3993180 NM_001079823.2:c.3154A>G