Allele Registry

Canonical Allele Identifier: PA220785

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000078788

RCV000805108

RCV000987776

ClinVar Variation:

92977

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.2:p.Phe2184Ser	CA220783 NM_000426.3:c.6551T>C