Allele Registry

Canonical Allele Identifier: PA2825167684

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000654730

RCV000764625

RCV004025934

ClinVar Variation:

543854

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Val1288Ile	CA3993373 NM_000426.4:c.3862G>A