Allele Registry

Canonical Allele Identifier: PA2825454408

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

521710

ClinVar RCV:

RCV000654725

RCV001155132

RCV003133470

ClinVar Variation:

543850

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Glu2792Asp	CA3994825 NM_001079823.2:c.8376A>C CA365634023 NM_001079823.2:c.8376A>T