Allele Registry

Canonical Allele Identifier: PA220782

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

98883

ClinVar RCV:

RCV000078787

RCV000665158

RCV002483133

RCV002513826

RCV004724798

ClinVar Variation:

92976

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.2:p.Arg2108Trp	CA220780 NM_000426.3:c.6322C>T