Allele Registry

Canonical Allele Identifier: PA234197

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000153431

RCV000623289

RCV001240997

ClinVar Variation:

167238

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.2:p.Pro208His	CA234195 NM_000426.3:c.623C>A