Allele Registry

Canonical Allele Identifier: PA2825167464

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

443878

ClinVar RCV:

RCV000522346

RCV000689663

RCV004541633

ClinVar Variation:

451960

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Ser1052Gly	CA3993180 NM_000426.4:c.3154A>G