Allele Registry

Canonical Allele Identifier: PA2825660200

Gene: LAMA3 HGNC NCBI

ClinVar RCV:

RCV000489231

RCV000675053

ClinVar Variation:

427194

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121190.2:p.Met822Leu	CA402056680 NM_001127718.2:c.2464A>C CA402056682 NM_001127718.2:c.2464A>T