Allele Registry

Canonical Allele Identifier: PA915967027

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000501465

RCV000535129

RCV000665212

RCV001153747

RCV001270112

RCV001507679

ClinVar Variation:

435712

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Trp739Cys	CA3992869 NM_001079823.2:c.2217G>T CA3992870 NM_001079823.2:c.2217G>C