Allele Registry

Canonical Allele Identifier: PA2573062627

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

521710

ClinVar RCV:

RCV000654725

RCV001155132

RCV003133470

ClinVar Variation:

543850

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Glu2796Asp	CA3994825 NM_000426.4:c.8388A>C CA365634023 NM_000426.4:c.8388A>T