Allele Registry

Canonical Allele Identifier: PA2825168429

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000363181

RCV000654772

RCV004544663

ClinVar Variation:

355285

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Tyr2069Cys	CA3994133 NM_000426.4:c.6206A>G