Allele Registry

Canonical Allele Identifier: PA2825167987

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

455361

ClinVar RCV:

RCV000525965

RCV003159942

ClinVar Variation:

477475

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Ile1596Val	CA3993668 NM_000426.4:c.4786A>G