Allele Registry

Canonical Allele Identifier: PA2825168276

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000518765

RCV000654769

RCV001154065

RCV001508564

ClinVar Variation:

447689

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Ala1897Thr	CA3993954 NM_000426.4:c.5689G>A