Allele Registry

Canonical Allele Identifier: PA2825167236

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000664485

RCV001049286

ClinVar Variation:

242608

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Thr821Pro	CA051537 NM_000426.4:c.2461A>C