Allele Registry

Canonical Allele Identifier: PA915967438

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000294738

RCV002061307

ClinVar Variation:

355277

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Trp1787Ser	CA3993854 NM_001079823.2:c.5360G>C