Allele Registry

Canonical Allele Identifier: PA2825166918

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000484636

ClinVar Variation:

421149

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Cys500Tyr	CA16618239 NM_000426.4:c.1499G>A