Allele Registry

Canonical Allele Identifier: PA2825166621

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000517812

RCV001591167

RCV001851444

ClinVar Variation:

447686

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Tyr163Phe	CA3992348 NM_000426.4:c.488A>T