Allele Registry

Canonical Allele Identifier: PA2825166598

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000505761

RCV000674785

RCV000802006

ClinVar Variation:

162573

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Ser146Phe	CA295383 NM_000426.4:c.437C>T