Allele Registry

Canonical Allele Identifier: PA2573062574

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

172229

ClinVar RCV:

RCV000149991

RCV000805156

RCV001156798

ClinVar Variation:

162581

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Arg2897Gln	CA295407 NM_000426.4:c.8690G>A