Canonical Allele Identifier: PA2825552899
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 406142
ClinVar RCV Id: RCV000467213 RCV004022586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098677.2:p.Cys1813Arg
CA3964708
NM_001105207.3:c.5437T>C