Allele Registry

Canonical Allele Identifier: PA2825168228

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

361443

ClinVar RCV:

RCV000415922

RCV000493358

RCV001080471

RCV001152793

RCV004544728

ClinVar Variation:

374557

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Arg1844Cys	CA3993905 NM_000426.4:c.5530C>T