Allele Registry

Canonical Allele Identifier: PA915965079

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

207314

ClinVar RCV:

RCV000192867

RCV000875855

RCV003129798

RCV004530131

ClinVar Variation:

211353

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Arg1674Lys	CA205986 NM_001079823.2:c.5021G>A