Allele Registry

Canonical Allele Identifier: PA915966981

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000724306

RCV001240233

ClinVar Variation:

194171

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Ile606Val	CA240011 NM_001079823.2:c.1816A>G