Allele Registry

Canonical Allele Identifier: PA2825167042

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000724306

RCV001240233

ClinVar Variation:

194171

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Ile606Val	CA240011 NM_000426.4:c.1816A>G