Canonical Allele Identifier: PA2741830339
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2549083
ClinVar RCV Id: RCV003268121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073291.2:p.Val2351Ile
CA3994425
NM_001079823.2:c.7051G>A