Allele Registry

Canonical Allele Identifier: PA2573176990

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV001940869

RCV003471076

ClinVar Variation:

1431679

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073291.2:p.Ser146Tyr	CA365829125 NM_001079823.2:c.437C>A