Allele Registry

Canonical Allele Identifier: PA2825167640

Gene: LAMA2 HGNC NCBI

ClinVar Variation Id: 2144139

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Phe1233Leu	CA365613056 NM_000426.4:c.3697T>C CA365613061 NM_000426.4:c.3699T>A CA365613062 NM_000426.4:c.3699T>G