Canonical Allele Identifier: PA645405802
Gene: LAMA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 406142
ClinVar RCV Id: RCV000467213 RCV004022586
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002281.3:p.Cys1813Arg
CA3964708
NM_002290.4:c.5437T>C