Allele Registry

Canonical Allele Identifier: PA915967500

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000224036

RCV000341200

RCV000522850

RCV000535681

ClinVar Variation:

235327

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Gln2043Arg	CA3994114 NM_001079823.2:c.6128A>G