Canonical Allele Identifier: PA2573177162
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1366792
ClinVar RCV Id: RCV001930213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Val991Ile
CA365611153
NM_001079823.2:c.2971G>A