Canonical Allele Identifier: PA2825168742
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1980729
ClinVar RCV Id: RCV002780323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Val2400Ile
CA146892066
NM_000426.4:c.7198G>A