Allele Registry

Canonical Allele Identifier: PA2825168716

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

425667

ClinVar RCV:

RCV000497710

RCV000699578

RCV003352895

ClinVar Variation:

432916

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Phe2371Cys	CA3994441 NM_000426.4:c.7112T>G