Allele Registry

Canonical Allele Identifier: PA2825168635

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000376263

RCV000700908

RCV000726647

RCV001266074

RCV002487558

ClinVar Variation:

355293

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Met2278Val	CA3994372 NM_000426.4:c.6832A>G