Allele Registry

Canonical Allele Identifier: PA2825660582

Gene: LAMA3 HGNC NCBI

ClinVar RCV:

RCV003554794

ClinVar Variation:

2726163

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121190.2:p.Lys1549Asn	CA8917248 NM_001127718.2:c.4647G>T CA402052146 NM_001127718.2:c.4647G>C