Allele Registry

Canonical Allele Identifier: PA915967502

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000178515

RCV000192788

RCV000509541

RCV000549092

RCV001154910

RCV001252049

RCV002516776

ClinVar Variation:

197478

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Gln2054Arg	CA205852 NM_001079823.2:c.6161A>G