Allele Registry

Canonical Allele Identifier: PA2825166454

Gene: LAMA2 HGNC NCBI

ClinVar RCV:

RCV000532735

RCV000672881

RCV001090685

ClinVar Variation:

477459

HGVS (amino-acid)	Matching Registered Transcripts
NP_000417.3:p.Met1Thr