Allele Registry

Canonical Allele Identifier: PA2825454458

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000179578

RCV002492787

RCV002515279

ClinVar Variation:

198300

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Asp2829Tyr	CA246861 NM_001079823.2:c.8485G>T