Allele Registry

Canonical Allele Identifier: PA2573062639

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000256378

RCV001814136

ClinVar Variation:

266017

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Gly2889Arg	CA10588944 NM_000426.4:c.8665G>A CA365634957 NM_000426.4:c.8665G>C