Allele Registry

Canonical Allele Identifier: PA2573062559

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000698683

ClinVar Variation:

576235

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Arg2578Gly	CA365628402 NM_000426.4:c.7732C>G