Allele Registry

Canonical Allele Identifier: PA2825166593

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV001940869

RCV003471076

ClinVar Variation:

1431679

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Ser146Tyr	CA365829125 NM_000426.4:c.437C>A