Allele Registry

Canonical Allele Identifier: PA915967076

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000664485

RCV001049286

ClinVar Variation:

242608

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Thr821Pro	CA051537 NM_001079823.2:c.2461A>C