Allele Registry

Canonical Allele Identifier: PA2829373678

Gene: LAMA4 HGNC NCBI

ClinVar RCV:

RCV000796863

RCV002345760

ClinVar Variation:

643208

HGVS (amino-acid)	Matching Registered Transcripts
NP_002281.3:p.Asn1745Asp	CA144877274 NM_002290.4:c.5233A>G