Allele Registry

Canonical Allele Identifier: PA2825551654

Gene: LAMA4 HGNC NCBI

ClinVar RCV:

RCV000600889

RCV001727778

RCV003372772

ClinVar Variation:

518375

HGVS (amino-acid)	Matching Registered Transcripts
NP_001098677.2:p.Trp14Arg	CA3966352 NM_001105207.3:c.40T>C CA365518971 NM_001105207.3:c.40T>A