Allele Registry

Canonical Allele Identifier: PA2825454056

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000015364

RCV003330391

ClinVar Variation:

14294

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Leu2560Pro	CA257207 NM_001079823.2:c.7679T>C