Allele Registry

Canonical Allele Identifier: PA2825167876

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000194655

RCV000509423

RCV000659062

RCV000709620

RCV001081183

RCV001152676

RCV004537432

ClinVar Variation:

196660

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Ala1496Val	CA208965 NM_000426.4:c.4487C>T