Allele Registry

Canonical Allele Identifier: PA2825552908

Gene: LAMA4 HGNC NCBI

ClinVar RCV:

RCV003837104

RCV004366887

ClinVar Variation:

2978442

HGVS (amino-acid)	Matching Registered Transcripts
NP_001098678.1:p.Trp7Leu	CA365519008 NM_001105208.3:c.20G>T