Allele Registry

Canonical Allele Identifier: PA2825167620

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000538799

RCV001508558

RCV004024401

ClinVar Variation:

477462

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Ile1210Val	CA3993321 NM_000426.4:c.3628A>G