Allele Registry

Canonical Allele Identifier: PA915966908

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000484636

ClinVar Variation:

421149

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Cys500Tyr	CA16618239 NM_001079823.2:c.1499G>A