Allele Registry

Canonical Allele Identifier: PA2825168567

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000178615

RCV001082197

RCV001152900

RCV004539671

ClinVar Variation:

197558

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Val2210Ala	CA245792 NM_000426.4:c.6629T>C