Allele Registry

Canonical Allele Identifier: PA2825166470

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000157587

RCV002469031

RCV002515056

ClinVar Variation:

180591

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Leu11Pro	CA273738 NM_000426.4:c.32T>C