Allele Registry

Canonical Allele Identifier: PA915967271

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000292683

RCV002523542

ClinVar Variation:

355266

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Asp1222Glu	CA3993326 NM_001079823.2:c.3666C>A CA365612951 NM_001079823.2:c.3666C>G