Allele Registry

Canonical Allele Identifier: PA915967136

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

443876

ClinVar RCV:

RCV000519809

RCV000702908

ClinVar Variation:

450118

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Gly923Ser	CA3993064 NM_001079823.2:c.2767G>A