Canonical Allele Identifier: PA2825168756
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543843
ClinVar RCV Id: RCV000654718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Thr2426Ile
CA365622156
NM_000426.4:c.7277C>T