Allele Registry

Canonical Allele Identifier: PA2825168483

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

521393

ClinVar RCV:

RCV000654759

ClinVar Variation:

543876

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Lys2117Arg	CA3994248 NM_000426.4:c.6350A>G