Canonical Allele Identifier: PA2825168748
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 906088
ClinVar RCV Id: RCV001155018 RCV001509286 RCV001242334 RCV001329267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Val2411Ile
CA3994489
NM_000426.4:c.7231G>A