Allele Registry

Canonical Allele Identifier: PA2825454549

Gene: LAMA2 HGNC NCBI

ClinVar Allele:

172229

ClinVar RCV:

RCV000149991

RCV000805156

RCV001156798

ClinVar Variation:

162581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Arg2893Gln	CA295407 NM_001079823.2:c.8678G>A