Canonical Allele Identifier: PA2825168672
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1208787
ClinVar RCV Id: RCV001577228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Lys2326Arg
CA365619424
NM_000426.4:c.6977A>G