Allele Registry

Canonical Allele Identifier: PA2825454841

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

428514

ClinVar RCV:

RCV000501974

RCV000824214

RCV001155233

RCV003133283

RCV004023380

ClinVar Variation:

435710

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Arg3081Gln	CA3995085 NM_001079823.2:c.9242G>A